IP Library › Granted Patent US 9,527,869
Granted Patent B2
US 9,527,869 · App. 14/741,965 · Granted Dec 27, 2016

Indolizine derivatives as phoshoinositide 3-kinases inhibitors

Inventors: Matteo Biagetti (Parma, IT); Alessandro Accetta (Parma, IT); Anna Maria Capelli (Parma, IT); Matilde Guala (Parma, IT); Michele Retini (Parma, IT)
Assignee: CHIESI FARMACEUTICI S.p.A.
C07D519/00A61K31/497A61K31/506A61K31/519A61K31/52A61K31/5377C07D471/04C07D473/02C07D487/04
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Quick Facts
Patent No.
US 9,527,869
App. No.
14/741,965
Granted
Dec 27, 2016
Kind
B2
Abstract

Compounds of formula (I), defined herein, inhibit phosphoinositide 3-kinases (PI3K) and are useful for the treatment of disorders associated with PI3K enzymes.

Claims (232)

1. A compound of formula (I)

wherein

X 1 , X 2 , X 3 and X 4 are all CH groups;

each R, when present, is —OR 5 , —SR 5 , —S(O) q —R 7 , halogen, —NR 10 R 11 , (C 1 -C 6 ) alkyl, (C 1 -C 6 ) haloalkyl, (C 1 -C 6 ) hydroxyalkyl, (C 1 -C 6 ) aminoalkyl, (C 3 -C 7 ) cycloalkyl, (C 2 -C 6 ) alkenyl, (C 5 -C 7 ) cycloalkenyl, (C 2 -C 6 ) alkynyl, (C 2 -C 6 ) hydroxyalkynyl, aryl, heteroaryl, or (C 3 -C 6 ) heterocycloalkyl, each of which may be optionally and independently substituted with one or more groups selected from the group consisting of halogen, —OH,(C 1 -C 6 ) alkyl, (C 1 -C 6 ) haloalkyl, (C 1 -C 6 ) hydroxyalkyl, (C 1 -C 6 ) aminoalkyl, (C 3 -C 7 ) cycloalkyl, (C 2 -C 6 ) alkenyl, (C 5 -C 7 ) cycloalkenyl, (C 2 -C 6 ) alkynyl, and (C 2 -C 6 ) hydroxyalkynyl;

R 1 is —H, —OR 6 , —SR 6 , —S(O) q —R 8 , halogen, —NR 12 R 13 , —CN, —C(O)NR 12 R 13 , —C(O)OR 16 , (C 1 -C 6 ) alkyl, (C 1 -C 6 ) haloalkyl, (C 1 -C 6 ) hydroxyalkyl, (C 1 -C 6 ) aminoalkyl, (C 3 -C 7 ) cycloalkyl, (C 2 -C 6 ) alkenyl, (C 5 -C 7 ) cycloalkenyl, (C 2 -C 6 ) alkynyl, (C 2 -C 6 ) hydroxyalkynyl, aryl, heteroaryl, or (C 3 -C 6 ) heterocycloalkyl, each of which may be optionally and independently substituted with one or more groups selected from the group consisting of halogen, —NR 22 R 23 , —(CH 2 ) n NR 22 R 23 , (C 1 -C 6 ) alkyl, (C 1 -C 6 ) alkoxyl, (C1-C6) aminoalkoxyl (C 3 -C 6 ) heterocycloalkyloxyl, (C 3 -C 6 ) heterocycloalkyl (C 1 -C 6 ) alkoxyl, (C 1 -C 6 ) haloalkyl, (C 1 -C 6 ) hydroxyalkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, and (C 2 -C 6 ) hydroxyalkynyl;

R 2 is —H, —OR 9 , —SR 9 , —S(O) q —R—, halogen, —NR 14 R 15 , —CN, —C(O)NR 14 R 15 , —C(O)OR 18 , —(C 1 -C 6 ) alkyl, —(C 1 -C 6 ) haloalkyl, —(C 1 -C 6 ) hydroxyalkyl, (C 1 -C 6 ) aminoalkyl, (C 3 -C 7 ) cycloalkyl, (C 5 -C 7 ) cycloalkenyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl,(C 2 -C 6 ) hydroxyalkynyl, aryl, heteroaryl, or (C 3 -C 6 ) heterocycloalkyl each of which may be optionally and independently substituted with one or more groups selected from the group consisting of halogen; —NR 24 R 25 , —(CH 2 ) n NR 24 R 25 , (C 1 -C 6 ) alkyl, (C 1 -C 6 ) haloalkyl,(C 1 -C 6 ) hydroxyalkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, and (C 2 -C 6 ) hydroxyalkynyl;

R 3 and R 4 , are the same or different and are each independently —H, (C 1 -C 6 ) alkyl, or (C 1 -C 6 ) haloalkyl;

Cy is 3H-purin-3-yl, 9H-purin-9-yl, 9H-purin-6-yl, 1H-pyrazolo[3,4-d]pyrimidin-1-yl, 6-oxo-5H,6H,7H-pyrrolo[2,3-d]pyrimidin-4-yl, pyrimidin-4-yl, pyrimidin-2-yl, pyrazin-2-yl, or 1,3,5-triazin-2-yl, each of which may be optionally and independently substituted by one or more substituents selected from the group consisting of halogen, —OH, —NR 19 R 20 , —CH 2 NR 19 R 20 ; —CN, —CH(O), —CH═NOH, —C(O)NR 19 R 20 , —C(O)OR 21 , (C 1 -C 6 ) alkyl, (C 1 -C 6 ) haloalkyl, (C 1 -C 6 ) hydroxyalkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, (C 2 -C 6 ) hydroxyalkynyl, aryl, heteroaryl, and (C 3 -C 6 ) heterocycloalkyl wherein each substituent may be optionally and independently substituted with one or more groups selected from the group consisting of —OH, halogen, —CN, —S(O) 2 NR I R III , —NR III S(O) 2 R II , —NR I R III , (C 1 -C 6 ) alkyl, (C 1 -C 6 ) haloalkyl, (C 1 -C 6 ) hydroxyalkyl, (C 1 -C 6 )alkoxy, aryl, heteroaryl, and (C 3 -C 6 ) heterocycloalkyl;

wherein R I R II and R III are the same or different and are each independently —H, (C 1 -C 6 ) alkyl or alkanoyl;

R 5 , R 6 , R 9 , R 16 , R 18 , and R 21 are the same or different and are each independently —H, (C 1 -C 6 ) alkyl, (C 1 -C 6 ) haloalkyl, (C 1 -C 6 ) hydroxyalkyl, (C 1 -C 6 ) aminoalkyl, alkanoyl, or aryl alkanoyl;

R 7 , R 8 and R 17 are the same or different and are each independently NR 12 R 13 , (C 1 -C 6 ) alkyl, (C 1 -C 6 ) haloalkyl, (C 1 -C 6 ) hydroxyalkyl, (C 1 -C 6 ) aminoalkyl, aryl, heteroaryl or(C 3 -C 6 ) heterocycloalkyl, each of which may be optionally and independently substituted with one or more groups selected from the group consisting of halogen, —NR 22 R 23 , —CH 2 NR 22 R 23 , (C 1 -C 6 ) alkyl, (C 1 -C 6 ) haloalkyl, (C 1 -C 6 ) hydroxyalkyl, (C 2 -C 6 ) alkenyl,(C 2 -C 6 ) alkynyl, and (C 2 -C 6 ) hydroxyalkynyl;

R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 19 , R 20 , R 22 , R 23 , R 24 and R 25 are the same or different and are each independently —H, (C 1 -C 6 ) alkyl, (C 1 -C 6 ) hydroxyalkyl, or alkanoyl or, taken together with the nitrogen atom to which they are bonded, anyone of R 10 and R 11 , R 12 and R 13 , R 14 and R 15 , R 19 and R 20 , R 22 and R 23 , abd R 24 and R 25 may form an optionally substituted 5 to 6 membered heterocycle wherein at least one ring carbon atom in said heterocycle may be replaced by at least one member selected from the group consisting of O, S, N, NH and an oxo substituent;

Z, when present, is —O—, —NH—, —C(O)—, —NHC(O)—, —C(O)NH—, —S—, —S(O)—, or —S(O) 2 —;

m is zero or 1;

n is 1 or 2;

p is zero or an integer ranging from 1 to 3; and

q is an integer ranging from 1 to 2,

or a pharmaceutically acceptable salt thereof.

2. A compound or pharmaceutically acceptable salt according to claim 1 , which is a mixture of diastereoisomers.

3. A compound or pharmaceutically acceptable salt according to claim 1 , wherein:

R 3 is H or (C 1 -C 6 ) alkyl; and

R 4 is H.

4. A compound or pharmaceutically acceptable salt according to claim 1 , wherein:

R 3 is (C 1 -C 6 ) alkyl;

R 4 is H.

5. A compound or pharmaceutically acceptable salt according to claim 1 , wherein:

R 3 is methyl;

R 4 is H; and

Cy is 1H-pyrazolo[3,4-d]pyrimidin-1-yl, which may be optionally substituted by one or more substituents selected from the group consisting of —NR 19 R 20 and aryl wherein said substituents may be optionally substituted by one or more groups selected from the group consisting of —OH and halogen.

6. A compound or pharmaceutically acceptable salt according to claim 5 , wherein:

R 1 is 4-morpholinomethyl, 2-methyl-2,9-diazaspiro[5.5]undecan-9-yl}methyl, 9-methyl-3,9-diazaspiro[5.5]undecan-3-yl}methyl, 7-methyl-2,7-diazaspiro[3.5]nonan-2-yl}methyl, or 5-methyl-octahydropyrrolo[3,4-c]pyrrol-2-yl]methyl;

R 3 is methyl;

R 4 is H; and

CY is 1H-pyrazolo[3,4-d]pyrimidin-1-yl (I-4), which is substituted in position 4 by —NH 2 and in position 3 by 3-fluoro-5-hydroxyphenyl.

7. A compound or pharmaceutically acceptable salt according to claim 1 , wherein:

R is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or halogen;

R 1 is hydrogen, C 2 -C 6 alkynyl, C 2 -C 6 aminoalkynyl, C 2 -C 6 hydroxyalkynyl, aryl, heteroaryl, C 3 -C 6 heterocycloalkyl, —(CH 2 ) n N 22 N 23 , wherein each aryl and heteroaryl may be optionally substituted by one or two groups independently selected from the group consisting of halogen, cyano, (C 1 -C 6 ) alkyl, —C(O)NR 12 R 13 , (C 3 -C 6 ) heterocycloalkyl, —NR 22 R 23 , —(CH 2 )nR 22 R 23 , (C 3 -C 6 ) heterocycloalkoxyl, and (C 3 -C 6 ) heterocycloalkyl (C 1 -C 6 ) alkoxyl;

R 2 is hydrogen, cyano, (C 1 -C 6 ) haloalkyl, aryl, or heteroaryl;

R 3 is H or (C 1 -C 6 ) alkyl;

R 4 is H;

Cy is 9H-purine-6-amine-9-yl, 3H-purine-6-amine-3-yl, 9H-purin-6-yl, 4-amino-5-cyanopyrimidin-6-yl, 4-amino-5-formylpyrimidin-6-yl, 4-amino-5-bromopyrimidin-6-yl, 4-amino-5-trifluoromethylpyrimidin-6-yl, 4-amino-5-methylpyrimidin-6-yl, 4-amino-5-(N-methtylcarbamoyl)pyrimidin-6-yl, 4-amino-5-carbamoylpyrimidin-6-yl, 4-amino-5-carboxypyrimidin-6-yl, 2-amino-3-pyrazinyl, 4-amino-5-hydroxymethylpyrimidin-6-yl, 4-amino-5-(4-morpholinomethyl)pyrimidin-6-yl, 4-amino-5-(hydroxyiminomethyl)pyrimidin-6-yl, 4-amino-5-(3-hydroxypropyn-1-yl)pyrimidin-6-yl, 4-amino-3-(3-fluoro-5-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-acetylaminophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-hydroxymethylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(5-hydroxy-3-trifluoromethylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-methanesulphonylaminophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-pyridyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(5-hydroxy-3-pyridyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-fluoro-4-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(4-fluoro-3-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-chloro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-aminosulphonylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-sulphonylamino-5-fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-aminosulphonyl-5-fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-amino-5-fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-cyano-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-fluoro-5-(1H-1,2,3,4-tetrazol-5-yl)phenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-hydroxypropyn-1-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, or 4-amino-3-(2-aminothiazol-5-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl.

m is 1;

n is 1;

p is 0 or 1; and

Z is absent or is —NH— or —NHC(O)—.

8. A compound or pharmaceutically acceptable salt according to claim 7 , wherein:

R is methyl, trifluoromethyl, or halogen selected from the group consisting of fluoro, chloro and bromo;

R 1 is hydrogen, 3-pent-1-yn-1-yl, 3-dimethylaminoprop-1-yn-1-yl, 3-hydroxyprop-1-yn-1-yl, phenyl, heteroaryl selected from the group consisting of pyridyl, pyrazinyl, thienyl and thiazolyl, 3,6-dihydro-2H-pyran-4-yl, 1,2,3,6-tetrahydropyridin-4-yl, pyrrolidin-1-yl-2-one, 4-methylpiperazin-1-yl-2-one, 4-morpholinomethyl, 2-methyl-2,9-diazaspiro[5.5]undecan-9-ylmethyl, 9-methyl-3,9-diazaspiro[5.5]undecan-3-yl}methyl, 7-methyl-2,7-diazaspiro[3.5]nonan-2-yl}methyl, and 5-methyl-octahydropyrrolo[3,4-c]pyrrol-2-yl]methyl, wherein each phenyl and heteroaryl may be optionally substituted by one or two groups independently selected from the group consisting of chlorine, fluorine, cyano, methyl, 4-morpholinocarbonyl, 1-methylpyrrolidin-1-yl, dimenthlamino, 2-dimethylaminomethyl, N,N-bis(2-hydroxyethyl)amino, 4-morpholinomethyl, 2-(4-morpholino)ethyl, 1-pyrrolidinomethyl, (4-methylpiperazin-1-yl)methyl, 1-methylpiperidin-4-yl-oxyl, 2-(4-methylpiperazin-1yl)ethoxyl, 2-(4-morpholino)ethoxyl, 2-dimethylaminoethoxyl and 2-(1-methylpiperidin-4-yl)ethoxyl;

R 2 is hydrogen, cyano, trifluoromethyl, phenyl which is optionally substituted by fluoro or methyl, or pyridinyl;

R 3 is H, methyl, or ethyl;

R 4 is H;

Cy is 9H-purine-6-amine-9-yl, 3H-purine-6-amine-3-yl, 9H-purin-6-yl, 4-amino-5-cyanopyrimidin-6-yl, 4-amino-5-formylpyrimidin-6-yl, 4-amino-5-bromopyrimidin-6-yl, 4-amino-5-trifluoromethylpyrimidin-6-yl, 4-amino-5-methylpyrimidin-6-yl, 4-amino-5-(N-methtylcarbamoyl)pyrimidin-6-yl, 4-amino-5-carbamoylpyrimidin-6-yl, 4-amino-5-carboxypyrimidin-6-yl, 2-amino-3-pyrazinyl, 4-amino-5-hydroxymethylpyrimidin-6-yl, 4-amino-5-(4-morpholinomethyl)pyrimidin-6-yl, 4-amino-5-(hydroxyiminomethyl)pyrimidin-6-yl, 4-amino-5-(3-hydroxypropyn-1-yl)pyrimidin-6-yl, 4-amino-3-(3-fluoro-5-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-acetylaminophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-hydroxymethylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(5-hydroxy-3-trifluoromethylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-methanesulphonylaminophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-pyridyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(5-hydroxy-3-pyridyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-fluoro-4-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(4-fluoro-3-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-chloro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-aminosulphonylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-sulphonylamino-5-fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-aminosulphonyl-5-fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-amino-5-fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-cyano-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-fluoro-5-(1H-1,2,3,4-tetrazol-5-yl)phenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, 4-amino-3-(3-hydroxypropyn-1-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl, or 4-amino-3-(2-aminothiazol-5-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl.

m is 1;

n is 1;

p is 0 or 1; and

Z is absent or is —NH— or —NHC(O)—.

9. A compound, which is selected from the group consisting of:

9-[(3-phenylindolizin-2-yl)methyl]-9H-purin-6-amine,

3-[(3-phenylindolizin-2-yl)methyl]-3H-purin-6-amine,

9-{[3-(pyridin-2-yl)indolizin-2-yl]methyl}-9H-purin-6-amine,

9-{[3-(3-fluorophenyl)indolizin-2-yl]methyl}-9H-purin-6-amine,

3-{[3-(3-fluorophenyl)indolizin-2-yl]methyl}-3H-purin-6-amine,

9-{[3-(2-fluorophenyl)indolizin-2-yl]methyl}-9H-purin-6-amine,

9-{[3-(2-methylphenyl)indolizin-2-yl]methyl}-9H-purin-6-amine,

3-{[3-(2-methylphenyl)indolizin-2-yl]methyl}-3H-purin-6-amine,

9-(indolizin-2-ylmethyl)-9H-purin-6-amine,

9-[(1-phenylindolizin-2-yl)methyl]-9H-purin-6-amine,

9-{[1-(3-fluorophenyl)indolizin-2-yl]methyl}-9H-purin-6-amine,

9-{[1-(2-methylphenyl)indolizin-2-yl]methyl}-9H-purin-6-amine,

N-[(3-phenylindolizin-2-yl)methyl]-9H-purin-6-amine,

N-{[3-(pyridin-2-yl)indolizin-2-yl]methyl}-9H-purin-6-amine,

N-{[3-(3-fluorophenyl)indolizin-2-yl]methyl}-9H-purin-6-amine,

N-{[3-(2-fluorophenyl)indolizin-2-yl]methyl}-9H-purin-6-amine,

N-[(1-phenylindolizin-2-yl)methyl]-9H-purin-6-amine,

N-{[1-(3-fluorophenyl)indolizin-2-yl]methyl}-9H-purin-6-amine,

N-{[1-(2-methylphenyl)indolizin-2-yl]methyl}-9H-purin-6-amine,

N-{[1-(pyridin-2-yl)indolizin-2-yl]methyl}-9H-purin-6-amine,

N-(indolizin-2-ylmethyl)-9H-purin-6-amine,

4-amino-6-{[(3-phenylindolizin-2-yl)methyl]amino}pyrimidine-5-carbonitrile,

4-amino-6-({[3-(pyridin-2-yl)indolizin-2-yl]methyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({[3-(3-fluorophenyl)indolizin-2-yl]methyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({[3-(2-fluorophenyl)indolizin-2-yl]methyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({[3-(2-methylphenyl)indolizin-2-yl]methyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-{[(1-phenylindolizin-2-yl)methyl]amino}pyrimidine-5-carbonitrile,

4-amino-6-({[1-(3-fluorophenyl)indolizin-2-yl]methyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({[1-(2-methylphenyl)indolizin-2-yl]methyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({[1-(pyridin-2-yl)indolizin-2-yl]methyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-[(indolizin-2-ylmethyl)amino]pyrimidine-5-carbonitrile,

4-amino-6-{[1-(3-phenylindolizin-2-yl)ethyl]amino}pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(pyridin-3-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(pyrazin-2-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(pyridin-4-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(thiophen-2-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(thiophen-3-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[8-fluoro-3-(pyridin-2-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[5-methyl-3-(pyridin-2-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[8-methyl-3-(pyridin-2-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(3,6-dihydro-2H-pyran-4-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(pent-1-yn-1-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(pyridin-2-yl)indolizin-2-yl]propyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(1,2,3,6-tetrahydropyridin-4-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(3-hydroxyprop-1-yn-1-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbonitrile,

4-amino-6-({1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carbaldehyde,

5-bromo-4-N-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}pyrimidine-4,6-diamine,

4-N-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-5-(trifluoromethyl)pyrimidine-4,6-diamine,

5-methyl-4-N-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}pyrimidine-4,6-diamine,

4-amino-N-methyl-6-({1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carboxamide,

4-amino-6-({1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carboxamide,

4-amino-6-({1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}amino)pyrimidine-5-carboxylic acid,

3-amino-N-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}pyrazine-2-carboxamide,

3-amino-N-{[1-(pyridin-2-yl)indolizin-2-yl]methyl}pyrazine-2-carboxamide,

[4-amino-6-({1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}amino)pyrimidin-5-yl]methanol,

5-(morpholin-4-ylmethyl)-4-N-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}pyrimidine-4,6-diamine,

5-[(1E)-(hydroxyimino)methyl]-4-N-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}pyrimidine-4,6-diamine,

3-[4-amino-6-({1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}amino)pyrimidin-5-yl]prop-2-yn-1-ol,

3-phenyl-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-4-amine,

3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)phenol,

3-(3-fluoro-5-methoxyphenyl)-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-4-amine,

N-[3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)phenyl]acetamide,

[3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)phenyl]methanol,

3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-(trifluoromethyl)phenol,

3-(3-fluorophenyl)-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-4-amine,

N-[3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)phenyl]methanesulfonamide,

1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-3-(pyridin-3-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine,

5-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)pyridin-3-ol,

4-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-2-fluorophenol,

5-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-2-fluorophenol,

3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-chlorophenol,

3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)benzene-1-sulfonamide,

N-[3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenyl]methanesulfonamide,

3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorobenzene-1-sulfonamide,

3-(3-amino-5-fluorophenyl)-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-4-amine,

3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-hydroxybenzonitrile,

3-[3-fluoro-5-(1H-1,2,3,4-tetrazol-5-yl)phenyl]-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-4-amine,

3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol enantiomer 1,

3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol enantiomer 2,

3-(4-amino-1-{1-[3-(pyridin-4-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-{4-amino-1-[1-(3-phenylindolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-(4-amino-1-{1-[3-(2-fluorophenyl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluoro-phenol,

3-(4-amino-1-{1-[6-methyl-3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{1-[3-(pyridin-2-yl)-6-(trifluoromethyl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{1-[1-methyl-3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-[4-amino-1-(1-{3-[5-(morpholin-4-ylmethyl)thiophen-2-yl]indolizin-2-yl}ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-5-fluorophenol,

3-[4-amino-1-(1-{3-[4-(morpholin-4-ylmethyl)phenyl]indolizin-2-yl}ethyl)-1H-indazol-3-yl]-5-fluorophenol,

3-{4-amino-1-[1-(3-{4-[(dimethylamino)methyl]phenyl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-{4-amino-1-[1-(3-{3-[(dimethylamino)methyl]phenyl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-{4-amino-1-[1-(3-{3-[(dimethylamino)methyl]phenyl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol enantiomer 1,

3-{4-amino-1-[1-(3-{3-[(dimethylamino)methyl]phenyl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol enantiomer 2,

3-(4-amino-1-{1-[3-(1,3-thiazol-5-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

1-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)pyrrolidin-2-one,

3-(4-amino-1-{1-[7-(pyridin-2-yl)pyrrolo[1,2-b]pyridazin-6-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{[3-(pyridin-2-yl)indolizin-2-yl]methyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{[3-(pyridin-3-yl)indolizin-2-yl]methyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{[3-(pyridin-4-yl)indolizin-2-yl]methyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{[7-(pyridin-2-yl)pyrrolo[1,2-b]pyridazin-6-yl]methyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{1-[3-(1,2,3,6-tetrahydropyridin-4-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)prop-2-yn-1-ol,

5-(4-amino-1-{1-[3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-1,3-thiazol-2-amine,

3-(4-amino-1-{1-[7-chloro-3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{1-[7-methyl-3-(pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{1-[3-(2-methylpyridin-4-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

5-(4-amino-1-{1-[3-(2-methylpyridin-4-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)pyridin-3-ol,

3-[4-amino-1-(1-{3-[5-(morpholin-4-ylmethyl)pyridin-2-yl]indolizin-2-yl}ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-5-fluorophenol,

3-[4-amino-1-(1-{3-[5-(morpholin-4-ylmethyl)pyridin-2-yl]indolizin-2-yl}ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-5-fluorophenol enantiomer 1,

3-[4-amino-1-(1-{3-[5-(morpholin-4-ylmethyl)pyridin-2-yl]indolizin-2-yl}ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-5-fluorophenol enantiomer 2,

3-{4-amino-1-[1-(3-{5-[(dimethylamino)methyl]pyridin-2-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-[4-amino-1-(1-{3-[6-(morpholin-4-ylmethyl)pyridin-2-yl]indolizin-2-yl}ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-5-fluorophenol,

3-[4-amino-1-(1-{3-[4-(morpholin-4-ylmethyl)pyridin-2-yl]indolizin-2-yl}ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-5-fluorophenol,

3-{4-amino-1-[1-(3-{4-[(dimethylamino)methyl]pyridin-2-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-[4-amino-1-(1-{3-[5-(pyrrolidin-1-ylmethyl)pyridin-2-yl]indolizin-2-yl}ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-5-fluorophenol,

3-{4-amino-1-[1-(3-{5-[(4-methylpiperazin-1-yl)methyl]pyridin-2-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-{4-amino-1-[1-(3-{5-[(4-methylpiperazin-1-yl)methyl]pyridin-2-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol enantiomer 1,

3-{4-amino-1-[1-(3-{5-[(4-methylpiperazin-1-yl)methyl]pyridin-2-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol enantiomer 2,

3-{4-amino-1-[1-(3-{6-[(4-methylpiperazin-1-yl)methyl]pyridin-2-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-{4-amino-1-[1-(3-{4-[(4-methylpiperazin-1-yl)methyl]pyridin-2-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-(4-amino-1-{1-[3-(5-{[bis(2-hydroxyethyl)amino]methyl}pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{1-[3-(5-{[bis(2-hydroxyethyl)amino]methyl}pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol enantiomer 1,

3-(4-amino-1-{1-[3-(5-{[bis(2-hydroxyethyl)amino]methyl}pyridin-2-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol enantiomer 2,

3-[4-amino-1-(1-{3-[3-(1-methylpyrrolidin-2-yl)phenyl]indolizin-2-yl}ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-5-fluorophenol,

3-{4-amino-1-[1-(3-{5-[2-(morpholin-4-yl)ethoxy]pyridin-2-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

5-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-1-[2-(morpholin-4-yl)ethyl]-1,2-dihydropyridin-2-one,

4-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-1-[2-(morpholin-4-yl)ethyl]-1,2-dihydropyridin-2-one,

4-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-1-[2-(morpholin-4-yl)ethyl]-1,2-dihydropyridin-2-one enantiomer 1,

4-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-1-[2-(morpholin-4-yl)ethyl]-1,2-dihydropyridin-2-one enantiomer 2,

4-(2-{1-[4-amino-3-(5-hydroxypyridin-3-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-1-[2-(morpholin-4-yl)ethyl]-1,2-dihydropyridin-2-one;

2-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)benzonitrile,

3-(4-amino-1-{1-[3-(pyridin-2-yl)-1-(trifluoromethyl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-[4-amino-1-(1-{3-[5-(morpholine-4-carbonyl)pyridin-2-yl]indolizin-2-yl}ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-5-fluorophenol,

2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}-3-(pyridin-2-yl)indolizine-1-carbonitrile,

2-{1-[4-amino-(3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}-3-{3-[(dimethylamino)methyl]phenyl}indolizine-1-carbonitrile,

2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}-3-{3-[(dimethylamino)methyl]phenyl}indolizine-1-carbonitrile enantiomer 1,

2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}-3-{3-[(dimethylamino)methyl]phenyl}indolizine-1-carbonitrile enantiomer 2,

3-{4-amino-1-[1-(7-{3-[(dimethylamino)methyl]phenyl}pyrrolo[1,2-b]pyridazin-6-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-(4-amino-1-{1-[3-(1,3-thiazol-4-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-[4-amino-1-(1-{3-[2-(morpholin-4-ylmethyl)-1,3-thiazol-4-yl]indolizin-2-yl}ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-5-fluorophenol,

3-[4-amino-1-(1-{3-[3-(dimethylamino)prop-1-yn-1-yl]indolizin-2-yl}ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-5-fluorophenol,

1-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-4-methylpiperazin-2-one,

4-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-1-[2-(dimethylamino)ethyl]-1,2-dihydropyridin-2-one,

4-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-1-[2-(dimethylamino)ethyl]-1,2-dihydropyridin-2-one enantiomer 1,

4-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-1-[2-(dimethylamino)ethyl]-1,2-dihydropyridin-2-one enantiomer 2,

6-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-2-[2-(pyrrolidin-1-yl)ethyl]-2,3-dihydropyridazin-3-one,

6-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-2-[2-(4-methylpiperazin-1-yl)ethyl]-2,3-dihydropyridazin-3-one,

6-(2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}indolizin-3-yl)-2-[2-(morpholin-4-yl)ethyl]-2,3-dihydropyridazin-3-one,

3-{4-amino-1-[1-(3-{6-[2-(4-methylpiperazin-1-yl)ethoxy]pyridazin-3-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-{4-amino-1-[1-(3-{6-[2-(dimethylamino)ethoxy]pyridazin-3-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-{4-amino-1-[1-(3-{6-[(1-methylpiperidin-4-yl)oxy]pyridazin-3-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-{4-amino-1-[1-(3-{6-[2-(1-methylpiperidin-4-yl)ethoxy]pyridazin-3-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-(4-amino-1-{1-[3-(morpholin-4-ylmethyl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{1-[3-({2-methyl-2,9-diazaspiro[5.5]undecan-9-yl}methyl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{1-[3-({9-methyl-3,9-diazaspiro[5.5]undecan-3-yl}methyl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-(4-amino-1-{1-[3-({7-methyl-2,7-diazaspiro[3.5]nonan-2-yl}methyl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol,

3-{1-[1-(3-{[(3aR,6aS)-5-methyl-octahydropyrrolo[3,4-c]pyrrol-2-yl]methyl}indolizin-2-yl)ethyl]-4-amino-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

2-{1-[4-amino-3-(3-fluoro-5-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}-3-(morpholin-4-ylmethyl)indolizine-1-carbonitrile,

3-{4-amino-1-[1-(3-{1-[2-(dimethylamino)ethyl]-1H-pyrazol-3-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-{4-amino-1-[1-(3-{1-[2-(4-methylpiperazin-1-yl)ethyl]-1H-pyrazol-3-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

3-(4-amino-1-{1-[3-(1-{2-[bis(2-hydroxyethyl)amino]ethyl}-1H-pyrazol-3-yl)indolizin-2-yl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5-fluorophenol, and

3-{4-amino-1-[1-(3-{1-[2-(morpholin-4-yl)ethyl]-1H-pyrazol-3-yl}indolizin-2-yl)ethyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluorophenol,

or a pharmaceutically acceptable salt of said compound.

10. A pharmaceutical composition, comprising a compound or pharmaceutically acceptable salt according to claim 1 in admixture with one or more pharmaceutically acceptable carriers or excipients.

11. A pharmaceutical composition according to claim 10 , further comprising one or more additional active agents.

12. A method for the treatment of rheumatoid arthritis, comprising administering, to a subject in need thereof, an effective amount of a compound or pharmaceutically acceptable salt according to claim 1 .

13. A method for treating asthma, chronic obstructive pulmonary disease, or idiopathic pulmonary fibrosis, comprising administering, to a subject in need thereof, an effective amount of a compound or pharmaceutically acceptable salt according to claim 1 .

14. A method for the treatment of rheumatoid arthritis, comprising administering, to a subject in need thereof, an effective amount of a compound or pharmaceutically acceptable salt according to claim 9 .

15. A method for treating asthma, chronic obstructive pulmonary disease, or idiopathic pulmonary fibrosis, comprising administering, to a subject in need thereof, an effective amount of a compound or pharmaceutically acceptable salt according to claim 9 .

16. A method for treating asthma, comprising administering, to a subject in need thereof, an effective amount of a compound or pharmaceutically acceptable salt according to claim 1 .

17. A method for treating asthma, comprising administering, to a subject in need thereof, an effective amount of a compound or pharmaceutically acceptable salt according to claim 9 .

18. A method for treating chronic obstructive pulmonary disease, comprising administering, to a subject in need thereof, an effective amount of a compound or pharmaceutically acceptable salt according to claim 1 .

19. A method for treating chronic obstructive pulmonary disease, comprising administering, to a subject in need thereof, an effective amount of a compound or pharmaceutically acceptable salt according to claim 9 .

20. A method for treating idiopathic pulmonary fibrosis, comprising administering, to a subject in need thereof, an effective amount of a compound or pharmaceutically acceptable salt according to claim 1 .

21. A method for treating idiopathic pulmonary fibrosis, comprising administering, to a subject in need thereof, an effective amount of a compound or pharmaceutically acceptable salt according to claim 9 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 10, 2016
From: BIAGETTI, MATTEO; ACCETTA, ALESSANDRO; CAPELLI, ANNA MARIA; GUALA, MATILDE; RETINI, MICHELE
To: CHIESI FARMACEUTICI S.P.A.
Reel/Frame 039974/0130 →
Priority Claims (1)
EP 14172764 · Jun 17, 2014 · regional
Continuity (1)
Related Publication 20150361100A1 · Dec 17, 2015