IP Library Granted Patent US 7,795,284
Granted Patent B2
US 7,795,284 · App. 11/718,791 · Granted Sep 14, 2010

4,7-dioxobenzothiazole-2-carboxamide derivatives, their preparation and their therapeutic uses

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,795,284
App. No.
11/718,791
Granted
Sep 14, 2010
Kind
B2
Abstract

A subject of the present invention is 4,7-dioxobenzothiazole-2-carboxamide derivatives, which inhibit the cdc25 phosphatases, in particular cdc25-C phosphatase. These compounds can in particular be used in the treatment of cancer.

Claims (78)

1. The compound of general formula (I)

in racemic, enantiomeric form or combination thereof, wherein:

R 1 is a hydrogen atom, alkyl, alkoxyalkyl, alkylthioalkyl, cycloalkyl, —(CH 2 )—X—Y, —(CH 2 )—Z—NR 6 R 7 radical or a —CHR 8 R 9 radical,

X is a bond or a linear or branched alkylene radical comprising 1 to 5 carbon atoms,

Y is a saturated cyclic carbon system comprising 1 to 3 condensed rings, wherein each ring independently comprises 3 to 7 members, or Y is a saturated heterocycle comprising 1 to 2 heteroatoms including O, N or S and attached to X by an N or CH member, said saturated heterocycle comprising 2 to 6 additional members, each independently including —CHR 10 —, —CO—, —NR 11 —, —O— or —S—, R 10 is a hydrogen atom or an alkyl radical and R 11 is a hydrogen atom or an alkyl or aralkyl radical, or Y is a carbocyclic or heterocyclic aryl radical optionally substituted by 1 to 3 substituents including a halogen atom, an alkyl radical, a haloalkyl radical, an alkoxy radical, a haloalkoxy radical, a hydroxy radical, a nitro radical, a cyano radical, a phenyl radical, an SO 2 NHR 12 radical or NR 13 R 14 radical, R 12 is a hydrogen atom or an alkyl or phenyl radical, and R 13 and R 14 are each independently-alkyl radicals,

Z is a bond or a linear or branched alkylene radical comprising 1 to 5 carbon atoms,

R 6 and R 7 are each independently a hydrogen atom, an alkyl, aralkyl or —(CH 2 ) n —OH radical, wherein n is an integer from 1 to 6,

or R 6 is an alkoxycarbonyl, haloalkoxycarbonyl or aralkoxycarbonyl radical and R 7 is a hydrogen atom or a methyl radical,

or R 6 and R 7 , together with the nitrogen atom to which they are attached, form a heterocycle with 4 to 7 members comprising 1 to 2 heteroatoms, wherein the members necessary for completing the heterocycle are each independently —CR 15 R 16 —, —O—, —S— or —NR 17 — radicals, R 15 and R 16 are each independently a hydrogen atom or an alkyl radical, and R 17 is a hydrogen atom, an alkyl, or aralkyl radical, or R 17 is a phenyl radical optionally substituted by 1 to 3 substituents including a halogen atom, an alkyl or alkoxy radical,

R 8 and R 9 , together with the carbon atom to which they are attached, form an indanyl or tetralinyl radical, or R 8 and R 9 , together with the carbon atom to which they are attached, form a saturated heterocycle comprising 5 to 7 members and 1 to 2 heteroatoms including O, N or S, wherein the nitrogen atoms of said heterocycle are optionally substituted by alkyl radicals or a benzyl radical;

R 2 is a hydrogen atom, an alkyl radical, or an aralkyl radical;

or R 1 and R 2 , together with the nitrogen atom to which they are attached, form a heterocycle with 4 to 8 members comprising 1 to 2 heteroatoms, wherein the members necessary for completing the heterocycle are each independently —CR 18 R 19 —, —O—, —S— or —NR 20 — radicals, R 18 and R 19 are each independently a hydrogen atom or an alkyl radical, and R 20 is a hydrogen atom, an alkyl radical, or an aralkyl radical;

R 3 represents is a hydrogen atom or a halogen atom;

R 4 is an alkyl radical, a haloalkyl radical, a cycloalkyl radical, a cycloalkylalkyl radical, an alkoxyalkyl radical, carbocyclic or heterocyclic aryl radicals or carbocyclic or heterocyclic aralkyl radicals the aryl nucleus of which is optionally substituted by 1 to 3 substituents independently including a halogen atom, an alkyl radical, an alkoxy radical, a haloalkyl radical or —SO 2 —NH 2 radical,

or R 4 is —(CH 2 ) m —[O—(CH 2 ) p ] q —O-Alk, —(CH 2 ) r —[O—(CH 2 ) s ] t —NR 21 R 22 or —(CH 2 ) v -A, wherein m, p and s are each independently an integer from 2 to 4, q is an integer from 1 to 4, t is an integer from 0 to 4, r is an integer from 2 to 12 and v is an integer from 1 to 12, Alk is an alkyl radical, R 21 is a hydrogen atoms, an alkyl, alkoxycarbonyl, or aralkoxycarbonyl radical, R 22 is a hydrogen atom or an alkyl radical and A is a saturated heterocycle comprising 1 to 2 heteroatoms independently including O, N or S and attached to the —(CH 2 ) v — group by an N or CH member, said saturated heterocycle including 2 to 6 additional members independently including —CHR 23 —, —CO—, —NR 24 —, —O— or —S—, R 23 is a hydrogen atom or an alkyl radical and R 24 is a hydrogen atom, an alkyl radical, an alkoxycarbonyl, or aralkoxycarbonyl group,

or R 4 is

wherein R 1 , R 2 , and R 3 are as defined above, and L is —(CH 2 ) g —[O—(CH 2 ) w ] x —[O—(CH 2 ) y ] z or —(CH 2 ) a -Ω-(CH 2 ) b —, wherein g, w and y are integers from 2 to 4, x is an integer from 1 to 3 and z is 0 or 1, a and b are independently integers from 2 to 6 and Ω is —O—, —S—, —NR 25 , —CO—, —CO—NR 26 —, —CR 27 R 28 —, a cycloalkylene radical containing 3 to 7 carbon atoms, or a carbocyclic aryl radical, R 25 is an alkyl radical, R 26 is a hydrogen atom or a methyl radical, R 27 and R 28 are each independently a hydrogen atom or a methyl group;

or R 4 is

R 5 is a hydrogen atom, an alkyl, or aralkyl radical, or R 5 is R 4 when R 4 is a carbocyclic or heterocyclic alkyl, haloalkyl, alkoxyalkyl or aralkyl radical, the aryl nucleus of which is optionally substituted by 1 to 3 substituents independently including a halogen atom, an alkyl radical, an alkoxy radical, a haloalkyl radical or —SO 2 —NH 2 radical;

or R 4 and R 5 , together with the nitrogen atom to which they are attached, form a saturated heterocycle with 4 to 7 members comprising 1 to 2 heteroatoms, wherein the members necessary for completing the heterocycle are each independently —CR 29 R 30 —, —O—, —S— or —NR 31 —, R 29 and R 30 are a hydrogen atom, an alkyl, or aralkyl radical and R 31 is —COR 32 or —SO 2 R 33 ,

R 32 is an alkyl radical, a carbocyclic aryl radical optionally substituted by 1 to 3 substituents including a halogen atom, an alkyl radical, or an alkoxy radical, or R 32 is a heterocyclic aryl radical or a saturated heterocycle comprising 5 to 7 members and 1 to 2 heteroatoms including O, N or S,

R 33 is a hydrogen atom or an alkyl radical,

or R 4 and R 5 , together with the nitrogen atom to which they are attached, form a heterocyclic aryl radical including

the aromatic ring of which may be substituted by 1 to 3 by substituents including an alkyl radical or an alkoxy radical;

or a salt thereof.

2. Compound according to claim 1 , wherein R 4 is not

or salt thereof.

3. Compound according to claim 1 , wherein R 4 is

or salt thereof.

4. Compound according to claim 1 , wherein the compound is:

5-{[2-(dimethylamino)ethyl]amino}-2-(morpholin-4-ylcarbonyl)-1,3-benzothiazole-4,7-dione;

tert-butyl{2-[2-(2-{[(5-{[2-(dimethylamino)ethyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazol-2-yl)carbonyl]amino}ethoxy)ethoxy]ethyl}carbamate;

N,N-dibenzyl-5-{[2-(dimethylamino)ethyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

5-{[2-(dimethylamino)ethyl]amino}-N,N-bis(2-methoxyethyl)-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

5-{[2-(dimethylamino)ethyl]amino}-4,7-dioxo-N-[3-(2-oxopyrrolidin-1-yl)propyl]-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

4,7-dioxo-N-[3-(2-oxopyrrolidin-1-yl)propyl]-5-[(2-pyrrolidin-1-ylethyl)amino]-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

5-{[2-(dimethylamino)ethyl]amino}-N-isobutyl-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

tert-butyl(4-{[(5-{[2-(dimethylamino)ethyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazol-2-yl)carbonyl]amino}butyl)carbamate;

5-{[2-(dimethylamino)ethyl]amino}-2-{[4-(2-furoyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

5-{[2-(dimethylamino)ethyl]amino}-N-(2-methoxyethyl)-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

N-butyl-5-{[2-(dimethylamino)ethyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

N-benzyl-5-{[2-(dimethylamino)ethyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

N-(cyclohexylmethyl)-5-{[2-(dimethylamino)ethyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

N,N′-(oxydiethane-2,1-diyl)bis(5-{[2-(dimethylamino)ethyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide);

N,N′-[ethane-1,2-diylbis(oxyethane-2,1-diyl)]bis(5-{[2-(dimethylamino)ethyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide);

5-{[2-(dimethylamino)ethyl]amino}-2-{[4-(morpholin-4-ylcarbonyl)piperazin-1-yl]carbonyl}1,3-benzothiazole-4,7-dione;

2-{[4-(morpholin-4-ylcarbonyl)piperazin-1-yl]carbonyl}-5-[(2-pyrrolidin-1-ylethyl)amino]1,3-benzothiazole-4,7-dione;

5-{[2-(dimethylamino)ethyl]amino}-N-(4-methoxyphenyl)-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

5-{[2-(dimethylamino)ethyl]amino}-2-{[4-(methylsulphonyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

5-{[2-(dimethylamino)ethyl]amino}-2-{[4-(tetrahydrofuran-2-ylcarbonyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

6-bromo-5-{[2-(dimethylamino)ethyl]amino}-2-{[4-(tetrahydrofuran-2-ylcarbonyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

5-{[2-(dimethylamino)ethyl]amino}-2-(pyrrolidin-1-ylcarbonyl)-1,3-benzothiazole-4,7-dione;

5-{[2-(dimethylamino)ethyl]amino}-2-{[4-(2-thienylcarbonyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

5-{[2-(dimethylamino)ethyl]amino}-N-ethyl-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

N-(4-chlorophenyl)-5-{[2-(dimethylamino)ethyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

N-1,3-benzodioxol-5-yl-5-{[2-(dimethylamino)ethyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

5-[(2-methoxyethyl)amino]-2-{[4-(tetrahydrofuran-2-ylcarbonyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

5-(4-methylpiperazin-1-yl)-2-{[4-(tetrahydrofuran-2-ylcarbonyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

5-[(2-pyridin-2-ylethyl)amino]-2-{[4-(tetrahydrofuran-2-ylcarbonyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

5-[(3-morpholin-4-ylpropyl)amino]-2-{[4-(tetrahydrofuran-2-ylcarbonyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

5-[(1-benzylpyrrolidin-3-yl)amino]-2-{[4-(tetrahydrofuran-2-ylcarbonyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

5-[(2-cyclohexylethyl)amino]-2-{[4-(tetrahydrofuran-2-ylcarbonyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

5-{[2-(dimethylamino)ethyl]amino}-N-(4-fluorophenyl)-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

6-{[2-(dimethylamino)ethyl]amino}-2-(pyrrolidin-1-ylcarbonyl)-1,3-benzothiazole-4,7-dione;

5-{[2-(dimethylamino)ethyl]amino}-N-(3-fluoro-4-methoxyphenyl)-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

5-{[2-{dimethylamino)ethyl]amino}-2-[(6-methoxy-3,4-dihydroquinolin-1(2H)-yl)carbonyl]-1,3-benzothiazole-4,7-dione;

5-{(2-(dimethylamino)ethyl]amino}-2-{[4-(4-methoxybenzoyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione;

5-{[2-(dimethylamino)ethyl](methyl)amino]-N-ethyl-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

N-ethyl-5-{[2-(4-fluorophenyl)ethyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide;

or salt thereof.

5. A pharmaceutical composition comprising a compound of formula (I) according to claim 1 or a pharmaceutically acceptable salt thereof. according to claim 1 or a pharmaceutically acceptable salt thereof.

6. A pharmaceutical composition comprising, as an active ingredient, a compound of formula (I) according to claim 1 or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.

7. A compound according to claim 1 , wherein the compound is 5-{[2-(dimethylamino)ethyl]amino}-2-{[4-(2-furoyl)piperazin-1-yl]carbonyl}-1,3-benzothiazole-4,7-dione.

8. A pharmaceutical composition comprising a compound of the formula according to claim 7 or a pharmaceutically acceptable salt thereof.

9. A pharmaceutical composition comprising, as an active ingredient, a compound of the formula according to claim 7 or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.

10. A compound according to claim 1 , wherein the compound is 6-{[2-(dimethylamino)ethyl]amino}-2-(pyrrolidin-1-ylcarbonyl)-1,3 -benzothiazole-4,7-dione.

11. A pharmaceutical composition comprising a compound of the formula according to claim 10 or a pharmaceutically acceptable salt thereof.

12. A pharmaceutical composition comprising, as an active ingredient, a compound of the formula according to claim 10 or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.

Assignments (4)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNOR NAME PREVIOUSLY RECORDED ON REEL 296336 FRAME 0777. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jan 5, 2016
From: SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES, S.A.S.
To: IPSEN PHARMA S.A.S.
Reel/Frame 037430/0194 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ADDRESS PREVIOUSLY RECORDED ON REEL 023034 FRAME 0251. ASSIGNOR(S) HEREBY CONFIRMS THE ADDRESS SHOULD BE 65 QUAI GEORGES GORSE, 92100 BOULOGNE-BILLANCOURT, FRANCE. Recorded Jan 16, 2013
From: SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATION SCIENTIFIQUES (S.C.R.A.S.)
To: IPSEN PHARMA S.A.S.
Reel/Frame 029636/0777 →
CHANGE OF NAME Recorded Jul 31, 2009
From: SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATION SCIENTIFIQUES (S.C.R.A.S.)
To: IPSEN PHARMA S.A.S.
Reel/Frame 023034/0251 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 16, 2007
From: GALCERA-CONTOUR, MARIE-ODILE; PREVOST, GREGOIRE; SIDHU, ALBAN
To: SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES
Reel/Frame 019967/0237 →