IP Library Granted Patent US 8,470,823
Granted Patent B2
US 8,470,823 · App. 13/060,718 · Granted Jun 25, 2013

Saturated bicyclic heterocyclic derivatives as SMO antagonists

Inventors: Danila Branca (Rome, IT); Federica Ferrigno (Rome, IT); Jose Ignacio Martin Hernando (Rome, IT); Philip Jones (Brookline, MA); Olaf Kinzel (Rome, IT); Savina Malancona (Rome, IT); Ester Muraglia (Rome, IT); Maria Cecilia Palumbi (Rome, IT); Giovanna Pescatore (Rome, IT); Rita Scarpelli (Rome, IT)
Assignee: Instituto di Ricerche di Biologia Molecolare P. Angeletti S.R.L.
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Quick Facts
Patent No.
US 8,470,823
App. No.
13/060,718
Granted
Jun 25, 2013
Kind
B2
Abstract

The present invention relates to compounds of formula I: and pharmaceutically acceptable salts or tautomers thereof which are inhibitors of the Sonic Hedgehog pathway, in particular Smoantagonists. Thus the compounds of this invention are useful for the treatment of diseases associated with abnormal hedgehog pathway activation, including cancer, for example basal cell carcinoma, medulloblastoma, prostate, pancreatic, breast, colon, bone and small cell lung cancers, and cancers of the upper GI tract.

Claims (39)

1. A compound of structural formula I:

wherein:

each of m and n is independently 1 or 2;

each of w, y and z is independently 0, 1 or 2;

x is 0 or 1;

A is C 3-7 cycloalkyl or fluoroC 3-7 cycloalkyl;

L is —(X═O) a (NR 7 ) b (O) c (CR 8 R 9 ) d (NR 7 ) e —;

a is 0 or 1;

b is 0 or 1;

c is 0 or 1;

d is 0, 1, 2, 3, 4, 5 or 6;

e is 0 or 1;

R 1 is C 1-6 alkyl, haloC 1-6 alkyl or a ring which is: C 6-10 aryl; C 3-10 cycloalkyl; oxetanyl; azetidinyl; a 5 or 6 membered saturated or partially saturated heterocyclic ring containing one, two or three heteroatoms independently selected from N, O and S; a 5 membered heteroaromatic ring containing 1, 2, 3 or 4 heteroatoms independently selected from N, O and S, not more than one heteroatom of which is O or S; a 6 membered heteroaromatic ring containing one, two or three N atoms; or a 7-15 membered unsaturated, partially saturated or saturated heterocyclic ring containing one, two, three or four heteroatoms independently selected from N, O and S; any of which rings being optionally substituted by one, two or three groups independently selected from R 10 ;

R 2 is a C 1-10 alkyl, haloC 1-10 alkyl, C 1-6 alkylmercaptoC 1-6 alkyl, C 2-10 alkenyl or a ring which is: C 3-10 cycloalkyl; C 6-10 aryl; oxetanyl; azetidinyl; a 5 or 6 membered saturated or partially saturated heterocyclic ring containing one, two or three heteroatoms independently selected from N, O and S; a 5 membered heteroaromatic ring containing 1, 2, 3 or 4 heteroatoms independently selected from N, O and S, not more than one heteroatom of which is O or S; a 6 membered heteroaromatic ring containing one, two or three N atoms; or a 7-15 membered saturated, partially saturated or unsaturated heterocyclic ring containing one, two, three or four heteroatoms independently selected from N, O and S; any of which rings being optionally substituted by one, two, three or four groups independently selected from R 11 ;

each of R 3 , R 4 , R 5 and R 6 is independently C 1-6 alkyl, C 2-10 alkenyl, haloC 1-6 alkyl, hydroxyC 1-6 alkyl, C 1-6 alkoxy, C 1-6 alkoxyC 1-6 alkyl, carboxy, CO 2 R a , CONR a R b , S(O) n R a or S(O) r NR a R b ;

r is 0, 1 or 2;

R 7 is hydrogen or C 1-6 alkyl;

each of R 8 and R 9 is independently hydrogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 alkoxycarbonyl or haloC 1-6 alkyl;

each R 10 is independently hydroxy, cyano, halogen, C 1-6 alkyl, haloC 1-6 alkyl, OR a or NR a R b ;

each R 11 is independently hydroxy, oxo, cyano, halogen, C 1-6 alkyl, C 1-6 alkylcarbonyl, C 2-10 alkenyl, C 2-10 alkynyl, haloC 1-6 alkyl, hydroxyC 1-6 alkyl, carboxy, nitro, OR a , NR a R b , NR a COR b , NR a S(O) n R b , NR a S(O) n NR a R b , CO 2 R a , CONR a R b , S(O) n R a , S(O) n NR a R b or a ring which is: C 3-10 cycloalkyl, C 6-10 aryl, C 6-10 aryloxy, C 6-10 arylC 1-6 alkoxy, C 6-10 arylC 1-6 alkyl, azetidinyl, a 5 or 6 membered saturated or partially saturated heterocyclic ring containing one, two or three heteroatoms independently selected from N, O and S, a 5 membered heteroaromatic ring containing 1, 2, 3 or 4 heteroatoms independently selected from N, O and S, not more than one heteroatom of which is O or S or a 6 membered heteroaromatic ring containing one, two or three N atoms; any of which rings being optionally substituted by one, two or three groups independently selected from hydroxy, oxo, cyano, halogen, C 1-6 alkyl, C 1-6 alkylsulfonyl, haloC 1-6 alkyl, C 1-6 alkoxy and haloC 1-6 alkoxy;

X is C or S═O;

each of R a and R b is independently hydrogen, C 1-6 alkyl, C 1-6 alkylcarbonyl, haloC 1-6 alkyl, hydroxyC 1-6 alkyl, C 3-10 cycloalkyl or C 6-10 aryl, any of which rings being optionally substituted by one, two or three groups independently selected from halogen and C 1-6 alkyl;

or a pharmaceutically acceptable salt, stereoisomer or tautomer thereof.

2. The compound of claim 1 of formula II:

wherein m, n, d, w, x, y, z, A, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 are as defined in claim 1 ;

or a pharmaceutically acceptable salt, stereoisomer or tautomer thereof.

3. The compound of claim 1 of formula IV:

wherein m, n, d, w, x, y, z, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 are as defined in claim 1 ;

or a pharmaceutically acceptable salt, stereoisomer or tautomer thereof.

4. The compound of claim 1 of formula V:

wherein d, w, x, y, z, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 are as defined in claim 1 ;

or a pharmaceutically acceptable salt, stereoisomer or tautomer thereof.

5. The compound of claim 1 of formula VII:

wherein d, w, x, y, z, R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are as defined in claim 1 ;

or a pharmaceutically acceptable salt, stereoisomer or tautomer thereof.

6. The compound of claim 1 wherein R 2 is C 1-8 alkyl, C 1-6 alkylmercaptoC 1-6 alkyl, C 2-6 alkenyl or a ring which is: phenyl, cyclohexyl, pyrazolyl, pyridinyl, benzodioxolyl, isoxazolyl, pyrrolidinyl, cyclopropyl, piperidinyl, tetrahydrothiopyranyl, oxazolyl, tetrahydronaphthalenyl, tetrahydroquinolinyl, tetrahydropyranyl, cyclopentyl or bicycloheptyl; any of which rings being optionally substituted by one, two or three groups independently selected from R 11 .

7. The compound of claim 1 wherein R 11 is cyano, halogen, C 1-6 alkyl, C 2-10 alkenyl, haloC 1-6 alkyl, OR a , NR a R b , CO 2 R a , S(O) r R a or a ring which is: C 6-10 aryl, C 6-10 arylC 1-6 alkoxy, or a 5 membered heteroaromatic ring containing 1, 2, 3 or 4 heteroatoms independently selected from N, O and S, not more than one heteroatom of which is O or S; any of which rings being optionally substituted by one, two or three groups independently selected from hydroxy, oxo, cyano, halogen, C 1-6 alkyl, haloC 1-6 alkyl, C 1-6 alkoxy and haloC 1-6 alkoxy.

8. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer or tautomer thereof in association with a pharmaceutically acceptable carrier.

9. A compound which is 8a-methyl-1,3-dioxo-2-[(1S,2R)-2-phenylcyclopropyl]-N-(1-phenyl-1H-pyrazol-5-yl)hexahydroimidazo[1,5-a]pyrazine-7(1H)-carboxamide and pharmaceutically acceptable salts, stereoisomers or tautomers thereof.

Assignments (3)
MERGER Recorded Apr 15, 2014
From: ISTITUTO DI RICERCHE DI BIOLOGIA MOLECOLARE P. ANGELETTI S.R.L.
To: MSD ITALIA S.R.L.
Reel/Frame 032672/0135 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY NAME: INSTITUTO DI RICERCHE DI BIOLOGIA MOLECOLARE P. ANGELETTI S.R.L. PREVIOUSLY RECORDED ON REEL 026121 FRAME 0271. ASSIGNOR(S) HEREBY CONFIRMS THE RECEIVING PARTY NAME: ISTITUTO DI RICERCHE DI BIOLOGIA MOLECOLARE P. ANGELETTI S.R.L.. Recorded Oct 11, 2013
From: BRANCA, DANILA; FERRIGNO, FEDERICA; HERNANDO, JOSE IGNACIO MARTIN; JONES, PHILIP; KINZEL, OLAF; MALANCONA, SAVINA; MURAGLIA, ESTER; PALUMBI, MARIA CECILIA; PESCATORE, GIOVANNA; SCARPELLI, RITA
To: ISTITUTO DI RICERCHE DI BIOLOGIA MOLECOLARE P. ANGELETTI S.R.L.
Reel/Frame 031397/0075 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2011
From: BRANCA, DANILA; FERRIGNO, FEDERICA; HERNANDO, JOSE IGNACIO MARTIN; JONES, PHILIP; KINZEL, OLAF; MALANCONA, SAVINA; MURAGLIA, ESTER; PALUMBI, MARIA CECILIA; PESCATORE, GIOVANNA; SCARPELLI, RITA
To: INSTITUTO DI RICERCHE DI BIOLOGIA MOLECOLARE P. ANGELETTI S.R.L.
Reel/Frame 026121/0271 →
Priority Claims (2)
GB 0815700.0 · Aug 29, 2008 · national
GB 0821817.4 · Nov 28, 2008 · national
Continuity (1)
Related Publication 20110183989A1 · Jul 28, 2011