SG183218A1 - Pyrrolopyrimidine compounds as inhibitors of cdk4/6 - Google Patents

Info

Publication number

SG183218A1

SG183218A1 SG2012058566A SG2012058566A SG183218A1 SG 183218 A1 SG183218 A1 SG 183218A1 SG 2012058566 A SG2012058566 A SG 2012058566A SG 2012058566 A SG2012058566 A SG 2012058566A SG 183218 A1 SG183218 A1 SG 183218A1

Authority

SG

Singapore

Prior art keywords

pyrrolo

ylamino

pyrimidine

pyridin

cyclopentyl

Prior art date

2010-02-19

Links

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• 150000004944 pyrrolopyrimidines Chemical class 0.000 title abstract description 6
• 239000003112 inhibitor Substances 0.000 title description 35
• 101100005789 Caenorhabditis elegans cdk-4 gene Proteins 0.000 title 1
• 238000000034 method Methods 0.000 claims abstract description 277
• 150000001875 compounds Chemical class 0.000 claims abstract description 184
• 150000003839 salts Chemical class 0.000 claims abstract description 79
• 206010028980 Neoplasm Diseases 0.000 claims abstract description 36
• 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 25
• 201000011510 cancer Diseases 0.000 claims abstract description 16
• QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 claims description 186
• 239000002253 acid Substances 0.000 claims description 158
• 229910052739 hydrogen Inorganic materials 0.000 claims description 70
• 229910052757 nitrogen Inorganic materials 0.000 claims description 35
• 125000000217 alkyl group Chemical group 0.000 claims description 33
• 229910052805 deuterium Inorganic materials 0.000 claims description 32
• YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical group [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 30
• 125000001424 substituent group Chemical group 0.000 claims description 29
• HKSQZEGSMBFHGC-UHFFFAOYSA-N pyrimidine-4-carboxamide Chemical compound NC(=O)C1=CC=NC=N1 HKSQZEGSMBFHGC-UHFFFAOYSA-N 0.000 claims description 23
• 239000001257 hydrogen Substances 0.000 claims description 20
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 9
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
• MGJXBDMLVWIYOQ-UHFFFAOYSA-N methylazanide Chemical compound [NH-]C MGJXBDMLVWIYOQ-UHFFFAOYSA-N 0.000 claims description 9
• FJWYXWJQDPCIEZ-UHFFFAOYSA-N 7-cyclopentyl-2-[[5-(3,8-diazabicyclo[3.2.1]octane-3-carbonyl)pyridin-2-yl]amino]-n,n-dimethylpyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound CN(C)C(=O)C1=CC2=CN=C(NC=3N=CC(=CC=3)C(=O)N3CC4CCC(N4)C3)N=C2N1C1CCCC1 FJWYXWJQDPCIEZ-UHFFFAOYSA-N 0.000 claims description 8
• VMHOCSPSLUBLHE-UHFFFAOYSA-N 7-cyclopentyl-2-[[5-(3,6-diazabicyclo[3.2.1]octane-3-carbonyl)pyridin-2-yl]amino]-n,n-dimethylpyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound CN(C)C(=O)C1=CC2=CN=C(NC=3N=CC(=CC=3)C(=O)N3CC4NCC(C4)C3)N=C2N1C1CCCC1 VMHOCSPSLUBLHE-UHFFFAOYSA-N 0.000 claims description 7
• 102100028651 Tenascin-N Human genes 0.000 claims description 7
• 101710087911 Tenascin-N Proteins 0.000 claims description 7
• BXALLQBVYDONPU-ICSRJNTNSA-N 2-[[5-[(3as,7ar)-6-oxo-2,3,3a,4,7,7a-hexahydro-1h-pyrrolo[3,4-c]pyridin-5-yl]pyridin-2-yl]amino]-7-cycloheptyl-n,n-dimethylpyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound CN(C)C(=O)C1=CC2=CN=C(NC=3N=CC(=CC=3)N3C(C[C@H]4CNC[C@H]4C3)=O)N=C2N1C1CCCCCC1 BXALLQBVYDONPU-ICSRJNTNSA-N 0.000 claims description 6
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
• 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
• 125000001188 haloalkyl group Chemical group 0.000 claims description 6
• 150000002431 hydrogen Chemical group 0.000 claims description 6
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 5
• WBCAOAIDJLJRCZ-UHFFFAOYSA-N 7-(3-tert-butylphenyl)-2-[[5-(3,8-diazabicyclo[3.2.1]octane-3-carbonyl)pyridin-2-yl]amino]-n,n-dimethylpyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound CN(C)C(=O)C1=CC2=CN=C(NC=3N=CC(=CC=3)C(=O)N3CC4CCC(N4)C3)N=C2N1C1=CC=CC(C(C)(C)C)=C1 WBCAOAIDJLJRCZ-UHFFFAOYSA-N 0.000 claims description 4
• HYLVNBXAOJUSTK-UHFFFAOYSA-N 7-cyclopentyl-2-[[5-(2,6-diazaspiro[3.3]heptane-2-carbonyl)pyridin-2-yl]amino]-n,n-dimethylpyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound N1=C2N(C3CCCC3)C(C(=O)N(C)C)=CC2=CN=C1NC(N=C1)=CC=C1C(=O)N(C1)CC21CNC2 HYLVNBXAOJUSTK-UHFFFAOYSA-N 0.000 claims description 4
• QUGUCRTXIGFAAB-UHFFFAOYSA-N 7-cyclopentyl-2-[[5-(3,8-diazabicyclo[3.2.1]octane-8-carbonyl)pyridin-2-yl]amino]-n,n-dimethylpyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound CN(C)C(=O)C1=CC2=CN=C(NC=3N=CC(=CC=3)C(=O)N3C4CCC3CNC4)N=C2N1C1CCCC1 QUGUCRTXIGFAAB-UHFFFAOYSA-N 0.000 claims description 4
• 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 4
• 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 4
• 239000000546 pharmaceutical excipient Substances 0.000 claims description 4
• PXFIUPLVBBAUKD-WMZOPIPTSA-N 2-[[5-[(3as,7ar)-6-oxo-2,3,3a,4,7,7a-hexahydro-1h-pyrrolo[3,4-c]pyridin-5-yl]pyridin-2-yl]amino]-7-cyclopentyl-n,n-dimethylpyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound CN(C)C(=O)C1=CC2=CN=C(NC=3N=CC(=CC=3)N3C(C[C@H]4CNC[C@H]4C3)=O)N=C2N1C1CCCC1 PXFIUPLVBBAUKD-WMZOPIPTSA-N 0.000 claims description 3
• YYUJVQQJCJMRSG-UHFFFAOYSA-N 7-[4-(2-cyanopropan-2-yl)phenyl]-2-[[5-(3,8-diazabicyclo[3.2.1]octane-8-carbonyl)pyridin-2-yl]amino]-n,n-dimethylpyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound CN(C)C(=O)C1=CC2=CN=C(NC=3N=CC(=CC=3)C(=O)N3C4CCC3CNC4)N=C2N1C1=CC=C(C(C)(C)C#N)C=C1 YYUJVQQJCJMRSG-UHFFFAOYSA-N 0.000 claims description 3
• JFBMZUGLNFOQBA-UHFFFAOYSA-N 7-cycloheptyl-2-[[5-(2,7-diazaspiro[3.5]nonane-7-carbonyl)pyridin-2-yl]amino]-n,n-dimethylpyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound N1=C2N(C3CCCCCC3)C(C(=O)N(C)C)=CC2=CN=C1NC(N=C1)=CC=C1C(=O)N(CC1)CCC21CNC2 JFBMZUGLNFOQBA-UHFFFAOYSA-N 0.000 claims description 3
• GAAOQIXOPLWYKD-UHFFFAOYSA-N 7-cyclopentyl-n,n-dimethyl-2-[[5-(2-oxo-1-oxa-3,9-diazaspiro[4.5]decan-3-yl)pyridin-2-yl]amino]pyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound N1=C2N(C3CCCC3)C(C(=O)N(C)C)=CC2=CN=C1NC(N=C1)=CC=C1N(C(O1)=O)CC21CCCNC2 GAAOQIXOPLWYKD-UHFFFAOYSA-N 0.000 claims description 3
• SBXGKKOSDIUNGQ-UHFFFAOYSA-N 7-cyclopentyl-n,n-dimethyl-2-[[5-(2-oxo-1-oxa-3,9-diazaspiro[4.6]undecan-3-yl)pyridin-2-yl]amino]pyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound N1=C2N(C3CCCC3)C(C(=O)N(C)C)=CC2=CN=C1NC(N=C1)=CC=C1N(C(O1)=O)CC21CCCNCC2 SBXGKKOSDIUNGQ-UHFFFAOYSA-N 0.000 claims description 3
• 229910052736 halogen Inorganic materials 0.000 claims description 3
• 150000002367 halogens Chemical class 0.000 claims description 3
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
• VTSDFHMWTKRCAL-UHFFFAOYSA-N 7-(4-tert-butylphenyl)-2-[[5-(3,8-diazabicyclo[3.2.1]octane-3-carbonyl)pyridin-2-yl]amino]-n,n-dimethylpyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound CN(C)C(=O)C1=CC2=CN=C(NC=3N=CC(=CC=3)C(=O)N3CC4CCC(N4)C3)N=C2N1C1=CC=C(C(C)(C)C)C=C1 VTSDFHMWTKRCAL-UHFFFAOYSA-N 0.000 claims description 2
• MGVGOHXTHDTWHQ-UHFFFAOYSA-N 7-cyclopentyl-2-[[5-(3,8-diazabicyclo[3.2.1]octane-3-carbonyl)-4-methylpyridin-2-yl]amino]-n,n-dimethylpyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound CN(C)C(=O)C1=CC2=CN=C(NC=3N=CC(=C(C)C=3)C(=O)N3CC4CCC(N4)C3)N=C2N1C1CCCC1 MGVGOHXTHDTWHQ-UHFFFAOYSA-N 0.000 claims description 2
• UHLMUTYUXRIVIZ-UHFFFAOYSA-N 7-cyclopentyl-n,n-dimethyl-2-[[5-(1-oxo-3,4,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazin-2-yl)pyridin-2-yl]amino]pyrrolo[2,3-d]pyrimidine-6-carboxamide Chemical compound CN(C)C(=O)C1=CC2=CN=C(NC=3N=CC(=CC=3)N3C(C4CCCN4CC3)=O)N=C2N1C1CCCC1 UHLMUTYUXRIVIZ-UHFFFAOYSA-N 0.000 claims description 2
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• 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
• 125000001475 halogen functional group Chemical group 0.000 claims 1
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract description 54
• 101000715943 Caenorhabditis elegans Cyclin-dependent kinase 4 homolog Proteins 0.000 abstract description 48
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