CA3017869C - Pyrazole aminopyrimidine derivatives as lrrk2 modulators - Google Patents
Pyrazole aminopyrimidine derivatives as lrrk2 modulators Download PDFInfo
- Publication number
- CA3017869C CA3017869C CA3017869A CA3017869A CA3017869C CA 3017869 C CA3017869 C CA 3017869C CA 3017869 A CA3017869 A CA 3017869A CA 3017869 A CA3017869 A CA 3017869A CA 3017869 C CA3017869 C CA 3017869C
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- CA
- Canada
- Prior art keywords
- methyl
- pyrazol
- trifluoromethyl
- diamine
- pyrimidine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- JOOFEGKZJOFZKJ-UHFFFAOYSA-N 1h-pyrazole;pyrimidin-2-amine Chemical class C=1C=NNC=1.NC1=NC=CC=N1 JOOFEGKZJOFZKJ-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 130
- 238000000034 method Methods 0.000 claims abstract description 81
- 150000003839 salts Chemical class 0.000 claims abstract description 34
- -1 C1-6alkoxy-C1-6alkyl Chemical group 0.000 claims description 375
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 190
- 125000000623 heterocyclic group Chemical group 0.000 claims description 115
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 77
- 238000006243 chemical reaction Methods 0.000 claims description 68
- 125000005843 halogen group Chemical group 0.000 claims description 63
- YAAWASYJIRZXSZ-UHFFFAOYSA-N pyrimidine-2,4-diamine Chemical compound NC1=CC=NC(N)=N1 YAAWASYJIRZXSZ-UHFFFAOYSA-N 0.000 claims description 63
- 229910052739 hydrogen Inorganic materials 0.000 claims description 62
- 239000001257 hydrogen Substances 0.000 claims description 60
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 52
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 40
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 40
- 230000008569 process Effects 0.000 claims description 35
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 33
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 32
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 31
- 125000001072 heteroaryl group Chemical group 0.000 claims description 30
- XVIAPHVAGFEFFN-UHFFFAOYSA-N pyrimidine-5-carbonitrile Chemical compound N#CC1=CN=CN=C1 XVIAPHVAGFEFFN-UHFFFAOYSA-N 0.000 claims description 29
- 125000003118 aryl group Chemical group 0.000 claims description 28
- 150000001412 amines Chemical class 0.000 claims description 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 25
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 24
- 229910052757 nitrogen Inorganic materials 0.000 claims description 21
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 claims description 21
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 20
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 17
- CKJNUZNMWOVDFN-UHFFFAOYSA-N methanone Chemical compound O=[CH-] CKJNUZNMWOVDFN-UHFFFAOYSA-N 0.000 claims description 16
- 239000002253 acid Substances 0.000 claims description 14
- 125000004429 atom Chemical group 0.000 claims description 14
- 239000003153 chemical reaction reagent Substances 0.000 claims description 14
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 13
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 13
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 12
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 11
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical group C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims description 11
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 9
- LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 claims description 9
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 9
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 8
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 7
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims description 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 7
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 7
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 7
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- 125000001246 bromo group Chemical group Br* 0.000 claims description 6
- 125000004043 oxo group Chemical group O=* 0.000 claims description 6
- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims description 5
- AUQDITHEDVOTCU-UHFFFAOYSA-N cyclopropyl cyanide Chemical compound N#CC1CC1 AUQDITHEDVOTCU-UHFFFAOYSA-N 0.000 claims description 5
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims description 5
- UFUASNAHBMBJIX-UHFFFAOYSA-N propan-1-one Chemical compound CC[C]=O UFUASNAHBMBJIX-UHFFFAOYSA-N 0.000 claims description 5
- 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims description 4
- 125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 claims description 4
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims description 4
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 4
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 claims description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- 125000002346 iodo group Chemical group I* 0.000 claims description 4
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 238000003786 synthesis reaction Methods 0.000 claims description 4
- 125000003158 alcohol group Chemical group 0.000 claims description 3
- GFBLFDSCAKHHGX-UHFFFAOYSA-N cyclobutanecarbonitrile Chemical compound N#CC1CCC1 GFBLFDSCAKHHGX-UHFFFAOYSA-N 0.000 claims description 3
- 229940080818 propionamide Drugs 0.000 claims description 3
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims description 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 2
- OXHNLMTVIGZXSG-UHFFFAOYSA-N 1-Methylpyrrole Chemical compound CN1C=CC=C1 OXHNLMTVIGZXSG-UHFFFAOYSA-N 0.000 claims description 2
- ZPPUMAMZIMPJGP-UHFFFAOYSA-N 2-methyl-2-[3-methyl-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]propanenitrile Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC=2C(=NN(C=2)C(C)(C)C#N)C)=N1 ZPPUMAMZIMPJGP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- CQLSMRRTGKFHDN-UHFFFAOYSA-N 4-[4-[[4-(ethylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]-5-methylpyrazol-1-yl]benzonitrile Chemical compound C1=C(C(F)(F)F)C(NCC)=NC(NC2=C(N(N=C2)C=2C=CC(=CC=2)C#N)C)=N1 CQLSMRRTGKFHDN-UHFFFAOYSA-N 0.000 claims description 2
- XWPKPKSGGUAEHZ-UHFFFAOYSA-N 5-chloro-4-methoxy-n-(5-methyl-1-phenylpyrazol-4-yl)pyrimidin-2-amine Chemical compound C1=C(Cl)C(OC)=NC(NC2=C(N(N=C2)C=2C=CC=CC=2)C)=N1 XWPKPKSGGUAEHZ-UHFFFAOYSA-N 0.000 claims description 2
- MGXHPPITINYTDB-UHFFFAOYSA-N 5-chloro-4-methoxy-n-[1-(2-methoxyethyl)-3-methylpyrazol-4-yl]pyrimidin-2-amine Chemical compound CC1=NN(CCOC)C=C1NC1=NC=C(Cl)C(OC)=N1 MGXHPPITINYTDB-UHFFFAOYSA-N 0.000 claims description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Substances CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000006299 oxetan-3-yl group Chemical group [H]C1([H])OC([H])([H])C1([H])* 0.000 claims description 2
- 125000004483 piperidin-3-yl group Chemical group N1CC(CCC1)* 0.000 claims description 2
- 239000002798 polar solvent Substances 0.000 claims description 2
- 239000003586 protic polar solvent Substances 0.000 claims description 2
- 125000006514 pyridin-2-ylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims description 2
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims description 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 3
- XBQUAYXWKXQAQK-UHFFFAOYSA-N 2-methyl-1-[3-methyl-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]propan-2-ol Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC=2C(=NN(CC(C)(C)O)C=2)C)=N1 XBQUAYXWKXQAQK-UHFFFAOYSA-N 0.000 claims 2
- NUWDQLQAMMOSMC-UHFFFAOYSA-N 2-n-[1-(2-methoxyethyl)-5-methylpyrazol-4-yl]-4-n-methyl-5-(trifluoromethyl)pyrimidine-2,4-diamine Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC2=C(N(CCOC)N=C2)C)=N1 NUWDQLQAMMOSMC-UHFFFAOYSA-N 0.000 claims 2
- VTKNOHUCAVQNQC-UHFFFAOYSA-N 2-n-[5-chloro-1-(3-fluoro-1-methylpiperidin-4-yl)pyrazol-4-yl]-4-n-methyl-5-(trifluoromethyl)pyrimidine-2,4-diamine Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC2=C(N(C3C(CN(C)CC3)F)N=C2)Cl)=N1 VTKNOHUCAVQNQC-UHFFFAOYSA-N 0.000 claims 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 2
- KXCWSMLDPVSABQ-NSHDSACASA-N (2s)-2-[3-methyl-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]-1-pyrrolidin-1-ylpropan-1-one Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC=2C(=NN(C=2)[C@@H](C)C(=O)N2CCCC2)C)=N1 KXCWSMLDPVSABQ-NSHDSACASA-N 0.000 claims 1
- VDMCENGCDUPAOP-ZETCQYMHSA-N (2s)-2-[3-methyl-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]propanenitrile Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC=2C(=NN(C=2)[C@@H](C)C#N)C)=N1 VDMCENGCDUPAOP-ZETCQYMHSA-N 0.000 claims 1
- RTIYNCIDRJGYFV-VIFPVBQESA-N (2s)-n,n-dimethyl-2-[5-methyl-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]propanamide Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC2=C(N([C@@H](C)C(=O)N(C)C)N=C2)C)=N1 RTIYNCIDRJGYFV-VIFPVBQESA-N 0.000 claims 1
- WSKNTCKMSASUDS-UHFFFAOYSA-N 1-[3-chloro-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]-2-methylpropan-2-ol Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC=2C(=NN(CC(C)(C)O)C=2)Cl)=N1 WSKNTCKMSASUDS-UHFFFAOYSA-N 0.000 claims 1
- GPYHHGOVZOCNTR-UHFFFAOYSA-N 1-[3-cyclopropyl-4-[[4-(ethylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]-2-methylpropan-2-ol Chemical compound C1=C(C(F)(F)F)C(NCC)=NC(NC=2C(=NN(CC(C)(C)O)C=2)C2CC2)=N1 GPYHHGOVZOCNTR-UHFFFAOYSA-N 0.000 claims 1
- ABZMZCOIHUNVOW-UHFFFAOYSA-N 1-[3-cyclopropyl-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]-2-methylpropan-2-ol Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC=2C(=NN(CC(C)(C)O)C=2)C2CC2)=N1 ABZMZCOIHUNVOW-UHFFFAOYSA-N 0.000 claims 1
- VCISAWBZRDSYAE-UHFFFAOYSA-N 1-[4-[4-[[4-(ethylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]-5-methylpyrazol-1-yl]piperidin-1-yl]-2-methylpropan-1-one Chemical compound C1=C(C(F)(F)F)C(NCC)=NC(NC2=C(N(C3CCN(CC3)C(=O)C(C)C)N=C2)C)=N1 VCISAWBZRDSYAE-UHFFFAOYSA-N 0.000 claims 1
- UNRCHRZMPHRCNO-UHFFFAOYSA-N 1-[4-[4-[[4-(ethylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]-5-methylpyrazol-1-yl]piperidin-1-yl]ethanone Chemical compound C1=C(C(F)(F)F)C(NCC)=NC(NC2=C(N(C3CCN(CC3)C(C)=O)N=C2)C)=N1 UNRCHRZMPHRCNO-UHFFFAOYSA-N 0.000 claims 1
- MAIPJZAUYBSGNY-UHFFFAOYSA-N 1-[4-[[4-(ethylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]-3-propan-2-ylpyrazol-1-yl]-2-methylpropan-2-ol Chemical compound C1=C(C(F)(F)F)C(NCC)=NC(NC=2C(=NN(CC(C)(C)O)C=2)C(C)C)=N1 MAIPJZAUYBSGNY-UHFFFAOYSA-N 0.000 claims 1
- KJZCKIGWOBSZIZ-UHFFFAOYSA-N 1-[5-chloro-4-[[4-(ethylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]-2-methylpropan-2-ol Chemical compound C1=C(C(F)(F)F)C(NCC)=NC(NC2=C(N(CC(C)(C)O)N=C2)Cl)=N1 KJZCKIGWOBSZIZ-UHFFFAOYSA-N 0.000 claims 1
- QVMQIGDQNDCVJU-UHFFFAOYSA-N 1-[5-chloro-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]cyclopropane-1-carbonitrile Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC2=C(N(N=C2)C2(CC2)C#N)Cl)=N1 QVMQIGDQNDCVJU-UHFFFAOYSA-N 0.000 claims 1
- QBIIPMKUEZQNFW-UHFFFAOYSA-N 2,2-dimethyl-3-[3-methyl-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]propanenitrile Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC=2C(=NN(CC(C)(C)C#N)C=2)C)=N1 QBIIPMKUEZQNFW-UHFFFAOYSA-N 0.000 claims 1
- JMPAUGJZZZVNSP-UHFFFAOYSA-N 2-[(1,3-dimethylpyrazol-4-yl)amino]-4-(methylamino)pyrimidine-5-carbonitrile Chemical compound C1=C(C#N)C(NC)=NC(NC=2C(=NN(C)C=2)C)=N1 JMPAUGJZZZVNSP-UHFFFAOYSA-N 0.000 claims 1
- DHBYPNGGSQZPSR-UHFFFAOYSA-N 2-[(1,5-dimethylpyrazol-4-yl)amino]-4-(methylamino)pyrimidine-5-carbonitrile Chemical compound C1=C(C#N)C(NC)=NC(NC2=C(N(C)N=C2)C)=N1 DHBYPNGGSQZPSR-UHFFFAOYSA-N 0.000 claims 1
- KMDGFQKNLCAUSR-UHFFFAOYSA-N 2-[(1,5-dimethylpyrazol-4-yl)amino]-4-methoxypyrimidine-5-carbonitrile Chemical compound C1=C(C#N)C(OC)=NC(NC2=C(N(C)N=C2)C)=N1 KMDGFQKNLCAUSR-UHFFFAOYSA-N 0.000 claims 1
- ZPJYLUOMTWDLAI-UHFFFAOYSA-N 2-[(1-ethyl-5-methylpyrazol-4-yl)amino]-4-(methylamino)pyrimidine-5-carbonitrile Chemical compound CCN1N=CC(NC=2N=C(NC)C(C#N)=CN=2)=C1C ZPJYLUOMTWDLAI-UHFFFAOYSA-N 0.000 claims 1
- OJEWMLUIKQSZPR-UHFFFAOYSA-N 2-[(1-ethyl-5-methylpyrazol-4-yl)amino]-4-methoxypyrimidine-5-carbonitrile Chemical compound CCN1N=CC(NC=2N=C(OC)C(C#N)=CN=2)=C1C OJEWMLUIKQSZPR-UHFFFAOYSA-N 0.000 claims 1
- FZYTYNCBJMMBBJ-UHFFFAOYSA-N 2-[3-cyclopropyl-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]-2-methylpropanenitrile Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC=2C(=NN(C=2)C(C)(C)C#N)C2CC2)=N1 FZYTYNCBJMMBBJ-UHFFFAOYSA-N 0.000 claims 1
- ZRWMINOKUFLOOK-UHFFFAOYSA-N 2-[3-ethyl-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]-2-methylpropanenitrile Chemical compound CCC1=NN(C(C)(C)C#N)C=C1NC1=NC=C(C(F)(F)F)C(NC)=N1 ZRWMINOKUFLOOK-UHFFFAOYSA-N 0.000 claims 1
- BQPOLMVAASMQGL-UHFFFAOYSA-N 2-[4-[(5-chloro-4-methoxypyrimidin-2-yl)amino]-3-cyclopropylpyrazol-1-yl]-2-methylpropanenitrile Chemical compound C1=C(Cl)C(OC)=NC(NC=2C(=NN(C=2)C(C)(C)C#N)C2CC2)=N1 BQPOLMVAASMQGL-UHFFFAOYSA-N 0.000 claims 1
- GPGVVCGTAPAQOE-UHFFFAOYSA-N 2-[4-[(5-chloro-4-methoxypyrimidin-2-yl)amino]-3-methylpyrazol-1-yl]-2-methylpropanenitrile Chemical compound C1=C(Cl)C(OC)=NC(NC=2C(=NN(C=2)C(C)(C)C#N)C)=N1 GPGVVCGTAPAQOE-UHFFFAOYSA-N 0.000 claims 1
- ZBHGYOPZGYZBQP-UHFFFAOYSA-N 2-[4-[(5-chloro-4-methoxypyrimidin-2-yl)amino]-5-methylpyrazol-1-yl]-2-methylpropanenitrile Chemical compound C1=C(Cl)C(OC)=NC(NC2=C(N(N=C2)C(C)(C)C#N)C)=N1 ZBHGYOPZGYZBQP-UHFFFAOYSA-N 0.000 claims 1
- JJLXBPFAWIFXLU-UHFFFAOYSA-N 2-[4-[[4-(ethylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]-3-methylpyrazol-1-yl]-n,2-dimethylpropanamide Chemical compound C1=C(C(F)(F)F)C(NCC)=NC(NC=2C(=NN(C=2)C(C)(C)C(=O)NC)C)=N1 JJLXBPFAWIFXLU-UHFFFAOYSA-N 0.000 claims 1
- OFEKPYXOGYKSGL-UHFFFAOYSA-N 2-[5-chloro-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]-n,2-dimethylpropanamide Chemical compound CNC(=O)C(C)(C)N1N=CC(NC=2N=C(NC)C(=CN=2)C(F)(F)F)=C1Cl OFEKPYXOGYKSGL-UHFFFAOYSA-N 0.000 claims 1
- YNKSAZBROVZCFY-UHFFFAOYSA-N 2-[[1-(3,5-difluorophenyl)-3-methylpyrazol-4-yl]amino]-4-(methylamino)pyrimidine-5-carbonitrile Chemical compound C1=C(C#N)C(NC)=NC(NC=2C(=NN(C=2)C=2C=C(F)C=C(F)C=2)C)=N1 YNKSAZBROVZCFY-UHFFFAOYSA-N 0.000 claims 1
- CWVWXGXXISZODW-UHFFFAOYSA-N 2-[[1-(3,5-difluorophenyl)-5-methylpyrazol-4-yl]amino]-4-(methylamino)pyrimidine-5-carbonitrile Chemical compound C1=C(C#N)C(NC)=NC(NC2=C(N(N=C2)C=2C=C(F)C=C(F)C=2)C)=N1 CWVWXGXXISZODW-UHFFFAOYSA-N 0.000 claims 1
- FUOHOCUYFKYXCL-UHFFFAOYSA-N 2-[[1-(4,4-difluorocyclohexyl)-3-methylpyrazol-4-yl]amino]-4-(methylamino)pyrimidine-5-carbonitrile Chemical compound C1=C(C#N)C(NC)=NC(NC=2C(=NN(C=2)C2CCC(F)(F)CC2)C)=N1 FUOHOCUYFKYXCL-UHFFFAOYSA-N 0.000 claims 1
- NFAQHHZFUVSCCL-UHFFFAOYSA-N 2-[[1-(4-chlorophenyl)-3-methylpyrazol-4-yl]amino]-4-(methylamino)pyrimidine-5-carbonitrile Chemical compound C1=C(C#N)C(NC)=NC(NC=2C(=NN(C=2)C=2C=CC(Cl)=CC=2)C)=N1 NFAQHHZFUVSCCL-UHFFFAOYSA-N 0.000 claims 1
- DXAUPORBZZSGBP-UHFFFAOYSA-N 2-[[1-(4-fluorophenyl)-3-methylpyrazol-4-yl]amino]-4-(methylamino)pyrimidine-5-carbonitrile Chemical compound C1=C(C#N)C(NC)=NC(NC=2C(=NN(C=2)C=2C=CC(F)=CC=2)C)=N1 DXAUPORBZZSGBP-UHFFFAOYSA-N 0.000 claims 1
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- XFRKATXKXCYIJI-UHFFFAOYSA-N 2-n-(1,5-dimethylpyrazol-4-yl)-4-n-methyl-5-(trifluoromethyl)pyrimidine-2,4-diamine Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC2=C(N(C)N=C2)C)=N1 XFRKATXKXCYIJI-UHFFFAOYSA-N 0.000 claims 1
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- GSXJKQFQEOCKST-UHFFFAOYSA-N 2-n-[1-(2-fluoroethyl)-5-methylpyrazol-4-yl]-4-n-methyl-5-(trifluoromethyl)pyrimidine-2,4-diamine Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC2=C(N(CCF)N=C2)C)=N1 GSXJKQFQEOCKST-UHFFFAOYSA-N 0.000 claims 1
- RNCMKOWVACJZQS-UHFFFAOYSA-N 2-n-[1-(2-methoxycyclopentyl)-3-methylpyrazol-4-yl]-4-n-methyl-5-(trifluoromethyl)pyrimidine-2,4-diamine Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC=2C(=NN(C=2)C2C(CCC2)OC)C)=N1 RNCMKOWVACJZQS-UHFFFAOYSA-N 0.000 claims 1
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- YKJFUBQPXZWRQL-UHFFFAOYSA-N 2-n-[1-(cyclopropylmethyl)-5-methylpyrazol-4-yl]-4-n-methyl-5-(trifluoromethyl)pyrimidine-2,4-diamine Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC2=C(N(CC3CC3)N=C2)C)=N1 YKJFUBQPXZWRQL-UHFFFAOYSA-N 0.000 claims 1
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- QKMHJNMVLOYTSC-QMMMGPOBSA-N 2-n-[1-[(2s)-2-methoxypropyl]-3-methylpyrazol-4-yl]-4-n-methyl-5-(trifluoromethyl)pyrimidine-2,4-diamine Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC=2C(=NN(C[C@H](C)OC)C=2)C)=N1 QKMHJNMVLOYTSC-QMMMGPOBSA-N 0.000 claims 1
- HJAUQNCGNYFLKU-UHFFFAOYSA-N 2-n-[1-[1-(1,3-dioxolan-2-ylmethyl)piperidin-4-yl]-3-methylpyrazol-4-yl]-4-n-ethyl-5-(trifluoromethyl)pyrimidine-2,4-diamine Chemical compound C1=C(C(F)(F)F)C(NCC)=NC(NC=2C(=NN(C=2)C2CCN(CC3OCCO3)CC2)C)=N1 HJAUQNCGNYFLKU-UHFFFAOYSA-N 0.000 claims 1
- DEKQSPVBLYHDOA-UHFFFAOYSA-N 2-n-[1-[1-(1,3-dioxolan-2-ylmethyl)piperidin-4-yl]-5-methylpyrazol-4-yl]-4-n-ethyl-5-(trifluoromethyl)pyrimidine-2,4-diamine Chemical compound C1=C(C(F)(F)F)C(NCC)=NC(NC2=C(N(C3CCN(CC4OCCO4)CC3)N=C2)C)=N1 DEKQSPVBLYHDOA-UHFFFAOYSA-N 0.000 claims 1
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- PUXPEQJKNAWNQA-UHFFFAOYSA-N 2-n-[5-chloro-1-[3-fluoro-1-(oxetan-3-yl)piperidin-4-yl]pyrazol-4-yl]-4-n-methyl-5-(trifluoromethyl)pyrimidine-2,4-diamine Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC2=C(N(C3C(CN(CC3)C3COC3)F)N=C2)Cl)=N1 PUXPEQJKNAWNQA-UHFFFAOYSA-N 0.000 claims 1
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- FSTSFBBVLTZZAP-UHFFFAOYSA-N 3-[5-chloro-4-[[4-(ethylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]-2,2-dimethylpropanenitrile Chemical compound C1=C(C(F)(F)F)C(NCC)=NC(NC2=C(N(CC(C)(C)C#N)N=C2)Cl)=N1 FSTSFBBVLTZZAP-UHFFFAOYSA-N 0.000 claims 1
- KULFBTUVKAKKJL-UHFFFAOYSA-N 3-methyl-1-[3-methyl-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]butan-2-ol Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC=2C(=NN(CC(O)C(C)C)C=2)C)=N1 KULFBTUVKAKKJL-UHFFFAOYSA-N 0.000 claims 1
- HVFKQKAMMMVYCV-UHFFFAOYSA-N 3-methyl-1-[5-methyl-4-[[4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]pyrazol-1-yl]butan-2-ol Chemical compound C1=C(C(F)(F)F)C(NC)=NC(NC2=C(N(CC(O)C(C)C)N=C2)C)=N1 HVFKQKAMMMVYCV-UHFFFAOYSA-N 0.000 claims 1
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- MASDDUOARPPIIU-UHFFFAOYSA-N 4-(2,2-difluoroethylamino)-2-[(1,5-dimethylpyrazol-4-yl)amino]pyrimidine-5-carbonitrile Chemical compound C1=NN(C)C(C)=C1NC1=NC=C(C#N)C(NCC(F)F)=N1 MASDDUOARPPIIU-UHFFFAOYSA-N 0.000 claims 1
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- IHCFFNSEOBOLFP-UHFFFAOYSA-N 4-(methylamino)-2-[(3-methyl-1-pyridin-2-ylpyrazol-4-yl)amino]pyrimidine-5-carbonitrile Chemical compound C1=C(C#N)C(NC)=NC(NC=2C(=NN(C=2)C=2N=CC=CC=2)C)=N1 IHCFFNSEOBOLFP-UHFFFAOYSA-N 0.000 claims 1
- ABNVVPZQDZUQDH-UHFFFAOYSA-N 4-(methylamino)-2-[(5-methyl-1-propan-2-ylpyrazol-4-yl)amino]pyrimidine-5-carbonitrile Chemical compound C1=C(C#N)C(NC)=NC(NC2=C(N(C(C)C)N=C2)C)=N1 ABNVVPZQDZUQDH-UHFFFAOYSA-N 0.000 claims 1
- PELWZUJUSISLDT-UHFFFAOYSA-N 4-(methylamino)-2-[[3-methyl-1-(2,2,2-trifluoroethyl)pyrazol-4-yl]amino]pyrimidine-5-carbonitrile Chemical compound C1=C(C#N)C(NC)=NC(NC=2C(=NN(CC(F)(F)F)C=2)C)=N1 PELWZUJUSISLDT-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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CA2812669A CA2812669C (en) | 2010-11-10 | 2011-11-09 | Pyrazole aminopyrimidine derivatives as lrrk2 modulators |
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