IP Library Granted Patent US 8,912,178
Granted Patent B2
US 8,912,178 · App. 13/698,501 · Granted Dec 16, 2014

mTOR selective kinase inhibitors

Inventor: Congxin Liang (Palm Beach Gardens, FL)
Assignee: Xcovery Holdings Company, LLC
C07D487/04
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Quick Facts
Patent No.
US 8,912,178
App. No.
13/698,501
Granted
Dec 16, 2014
Kind
B2
Abstract

The 4-urea-phenyl substituted 6-morpholin-4-yl-pyrazolo[3,4-d]pyrimidine derivatives are potent and selective inhibitors of mTOR kinase and are useful in treating disorders related to abnormal mTOR activities such as cancer, immune disorders, cardiovascular disease, ocular disease, viral infection, inflammation, metabolism/endocrine disorders and neurological disorders.

Claims (53)

1. A compound of Formula II:

or a salt thereof; wherein X is CH;

R 1 is 1 ) heterocyclyl optionally substituted with C(O)OR 15 , C(O)R 16 , or S(O) 2 R 17 ; or 2) cycloalkyl optionally substituted with OH, C(O)OR 15 , or R 17 ;

R 2 is hydrogen or alkyl;

R 3 is hydrogen;

each R 4 is independently 1) alkyl; or 2) aryl optionally substituted with R 16 or C(O)R 16 ;

R 5 is hydrogen; or each R 2 and R 5 together with the atom(s) that each is respectively attached to can form a cyclo or heterocyclo structure;

R 15 is hydrogen or C 1 -C 4 alkyl;

R 16 is heterocyclyl or C 1 -C 4 alkyl, wherein each of said heterocyclyl or C 1 -C 4 alkyl is independently optionally substituted with OH, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, or NH 2 ; and

R 17 is C 1 -C 4 alkyl optionally substituted with OH.

2. The compound of claim 1 , wherein R 2 and R 5 together with the atoms to which they are attached form a heterocycloalkyl.

3. The compound of claim 1 , wherein R 1 is heterocyclyl optionally substituted with C(O)OR 15 , C(O)R 16 , or S(O) 2 R 17 ;

R 15 is hydrogen or C 1 -C 4 alkyl;

R 16 is heterocyclyl or C 1 -C 4 alkyl, wherein each of said heterocyclyl or C 1 -C 4 alkyl is independently optionally substituted with OH, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, or NH 2 ; and

R 17 is C 1 -C 4 alkyl.

4. The compound of claim 1 , wherein R 1 is cycloalkyl optionally substituted with OH, C(O)OR 15 , or R 17 ;

R 15 is hydrogen or C 1 -C 4 alkyl; and

R 17 is C 1 -C 4 alkyl substituted with OH.

5. The compound of claim 1 , wherein R 4 is alkyl.

6. The compound of claim 1 , wherein R 4 is aryl optionally substituted with R 16 or C(O)R 16 ; and

R 16 is heterocyclyl or C 1 -C 4 alkyl, wherein each of said heterocyclyl or C 1 -C 4 alkyl is independently optionally substituted with OH, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, or NH 2 .

7. The compound of claim 1 , wherein R 4 is aryl substituted with —C(O)R 16 ; and

R 16 is heterocyclyl or C 1 -C 4 alkyl, wherein each of said heterocyclyl or C 1 -C 4 alkyl is independently optionally substituted with OH, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, or NH 2 .

8. The compound of claim 7 , wherein R 16 is heterocyclyl substituted with C 1 -C 4 alkyl.

9. The compound of claim 1 , wherein R 4 is aryl substituted with heterocyclyl.

10. The compound of claim 1 , wherein;

R 1 is heterocyclyl optionally substituted with C(O)OR 15 , C(O)R 16 , or S(O) 2 R 17 ;

R 4 is alkyl;

R 15 is hydrogen or C 1 -C 4 alkyl;

R 16 is heterocyclyl or C 1 -C 4 alkyl, wherein each of said heterocyclyl or C 1 -C 4 alkyl is independently optionally substituted with OH, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, or NH 2 ; and

R 17 is alkyl.

11. The compound of claim 1 , wherein the compound is one of methyl 4-[4-[4-(methylcarbamoylamino)phenyl]-6-morpholino-pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate;

1-methyl-3-[4-[1-[1-(4-methylpiperazine-1- carbonyl)-4-piperidyl]-6-morpholino-pyrazolo[3,4-d]pyrimidin-4-yl]phenyl]urea;

1-[4-[1-[1-[(2S)-2-aminopropanoyl]-4-piperidyl]-6-morpholino-pyrazolo[3,4-d]pyrimidin-4-yl]phenyl]-3-methyl-urea;

1-[4-[1-[1-(2-hydroxyacetyl)-4-piperidyl]-6-morpholino-pyrazolo[3,4-d]pyrimidin-4-yl]phenyl]-3-methyl-urea;

1-[4-[1-[1-[(2S)-2-hydroxypropanoyl]-4-piperidyl]-6-morpholino-pyrazolo[3,4-d]pyrimidin-4-yl]phenyl]-3-methylurea;

1-[4-[1-[1-(2-methoxyacetyl)-4-piperidyl]-6-morpholino-pyrazolo[3,4-d]pyrimidin-4-yl]phenyl]-3-methyl-urea;

1-methyl-3-[4-[1-(1-methylsulfonyl-4-piperidyl)-6-morpholino-pyrazolo[3,4-d]pyrimidin-4-yl]phenyl]urea;

1-methyl-3-[4-(6-morpholino-1-tetrahydropyran-4-yl-pyrazolo[3,4-d]pyrimidin-4-yl)phenyl]urea;

1-methyl-3-[4-[6-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-tetrahydropyran-4-yl-pyrazolo[3,4-d]pyrimidin-4-yl]phenyl]urea;

1-methyl-3-[4-[6-[(3S)-3-methylmorpholin-4-yl]-1-tetrahydropyran-4-yl-pyrazolo[3,4-d]pyrimidin-4-yl]phenyl]urea;

N-{4-[1-(2H-3,4,5,6-tetrahydropyran-4-yl)-6-((3R)-3-methylmorpholin-4-yl)pyrazolo[4,5-e]pyrimidin-4-yl]phenyl}(methylamino)carboxamide;

ethyl 4-(4-{4-[(methylamino)carbonylamino]phenyl}-6-morpholin-4-yl pyrazolo[5,4-d]pyrimidinyl)cyclohexanecarboxylate;

N-(4-{1-[4-(hydroxymethyl)cyclohexyl]-6-morpholin-4-ylpyrazolo[4,5-e]pyrimidin-4-yl}phenyl)(methylamino)carboxamide;

4-(4-{4-[(methylamino)carbonylamino]phenyl}-6-morpholin-4-yl pyrazolo[5,4-d]pyrimidinyl)cyclohexanecarboxylic acid;

N-{4-[1-(4-hydroxycyclohexyl)-6-morpholin-4-ylpyrazolo[4,5-e]pyrimidin-4-yl]phenyl}(methylamino)carboxamide;

4-[6-((3S)-3-methylmorpholin-4-yl)-4-(4-aminophenyl)pyrazolo[5,4-d]pyrimidinyl]cyclohexan-1-ol;

N-[4-(1-cyclopentyl-6-morpholin-4-ylpyrazolo[4,5-e]pyrimidin-4-yl) phenyl](methylamino)carboxamide;

N-{4-[6-((3S)-3-methylmorpholin-4-yl)-1- cyclopentylpyrazolo[4,5-e]pyrimidin-4-yl]phenyl}(methylamino)carboxamide;

N-{4-[1-(4-hydroxycyclohexyl)-6-morpholin-4-ylpyrazolo[4,5-e]pyrimidin-4-yl]phenyl}(methylamino)carboxamide(cis);

N-{4-[1-(4-hydroxycyclohexyl)-6-morpholin-4-ylpyrazolo[4,5-e]pyrimidin-4-yl]phenyl}(methylamino)carboxamide(trans);

1-[4-(6-morpholino-1-tetrahydropyran-4-yl-pyrazolo[3,4-d]pyrimidin-4-yl)phenyl]-3-(2,2,2-trifluoroethyl)urea;

1-[4-[6-[(3S)-3-methylmorpholin-4-yl]-1-tetrahydropyran-4-yl-pyrazolo[3,4-d]pyrimidin-4-yl]phenyl]-3-(2,2,2-trifluoroethyl)urea.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2014
From: LIANG, CONGXIN
To: XCOVERY HOLDING COMPANY, LLC
Reel/Frame 032653/0427 →
Continuity (2)
Provisional Application 61346278 · May 19, 2010
Related Publication 20130072481A1 · Mar 21, 2013