JP2017519772A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2017519772A5 JP2017519772A5 JP2016574242A JP2016574242A JP2017519772A5 JP 2017519772 A5 JP2017519772 A5 JP 2017519772A5 JP 2016574242 A JP2016574242 A JP 2016574242A JP 2016574242 A JP2016574242 A JP 2016574242A JP 2017519772 A5 JP2017519772 A5 JP 2017519772A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- piperidin
- quinazolin
- cyclopropyl
- phenyl
- 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.)
- Granted
Links
- 229910052739 hydrogen Inorganic materials 0.000 claims 36
- 239000001257 hydrogen Substances 0.000 claims 36
- 125000000217 alkyl group Chemical group 0.000 claims 29
- 150000002431 hydrogen Chemical class 0.000 claims 27
- 150000003839 salts Chemical class 0.000 claims 24
- 150000001875 compounds Chemical class 0.000 claims 23
- 239000000651 prodrug Substances 0.000 claims 23
- 229940002612 prodrug Drugs 0.000 claims 23
- 239000012453 solvate Substances 0.000 claims 23
- 150000001204 N-oxides Chemical class 0.000 claims 19
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 18
- 229910052736 halogen Inorganic materials 0.000 claims 18
- 150000002367 halogens Chemical class 0.000 claims 18
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 13
- 125000003545 alkoxy group Chemical group 0.000 claims 12
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 9
- 229910052757 nitrogen Inorganic materials 0.000 claims 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims 8
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 7
- -1 2-Dimethylamino-phenyl Chemical group 0.000 claims 5
- 229910052799 carbon Inorganic materials 0.000 claims 5
- 208000035475 disorder Diseases 0.000 claims 5
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- SQSASMLYFCBHPV-OAQYLSRUSA-N (3R)-1-[2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]pyrrolidin-3-ol Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N1C[C@@H](CC1)O SQSASMLYFCBHPV-OAQYLSRUSA-N 0.000 claims 3
- 125000006420 1-fluorocyclopropyl group Chemical group [H]C1([H])C([H])([H])C1(F)* 0.000 claims 3
- JPWQBXUIRBWWIL-JOCHJYFZSA-N 2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]-6-[(3R)-3-methoxypyrrolidin-1-yl]quinazoline Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N1C[C@@H](CC1)OC JPWQBXUIRBWWIL-JOCHJYFZSA-N 0.000 claims 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 3
- SQSASMLYFCBHPV-NRFANRHFSA-N (3S)-1-[2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]pyrrolidin-3-ol Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N1C[C@H](CC1)O SQSASMLYFCBHPV-NRFANRHFSA-N 0.000 claims 2
- ZIZNYROAMFIPDX-FQEVSTJZSA-N (3S)-1-[8-chloro-2-(1-fluorocyclobutyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]pyrrolidin-3-ol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=C(Cl)C=C(C=C12)N1CC[C@H](O)C1)C1(F)CCC1 ZIZNYROAMFIPDX-FQEVSTJZSA-N 0.000 claims 2
- FMFRQMRIYSDVQZ-UHFFFAOYSA-N 1-[2-(1-fluorocyclobutyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]pyrido[3,4-d]pyrimidin-6-yl]pyrrolidin-3-ol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=C2C=C(N=CC2=NC(=N1)C1(F)CCC1)N1CCC(O)C1 FMFRQMRIYSDVQZ-UHFFFAOYSA-N 0.000 claims 2
- FDWXBJUKEDKWII-UHFFFAOYSA-N 1-[2-(1-fluorocyclopropyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]pyrido[3,4-d]pyrimidin-6-yl]pyrrolidin-3-ol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=C2C=C(N=CC2=NC(=N1)C1(F)CC1)N1CCC(O)C1 FDWXBJUKEDKWII-UHFFFAOYSA-N 0.000 claims 2
- 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 claims 2
- MMDSVKYAQRIDEA-UHFFFAOYSA-N 2-[[2-(1-fluorocyclobutyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CCC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCO)C MMDSVKYAQRIDEA-UHFFFAOYSA-N 0.000 claims 2
- YOJPYKIAGMVMSR-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]pyrido[3,4-d]pyrimidin-6-yl]-methylamino]ethanol Chemical compound FC1(CC1)C=1N=C(C2=C(N=1)C=NC(=C2)N(CCO)C)N1CCC(CC1)C1=C(C=CC=C1)OC YOJPYKIAGMVMSR-UHFFFAOYSA-N 0.000 claims 2
- BLWXTJQMEBQCIZ-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCO)C BLWXTJQMEBQCIZ-UHFFFAOYSA-N 0.000 claims 2
- VDPVHNVRGBBVTG-UHFFFAOYSA-N 2-[[2-cyclopropyl-4-[4-(3-methoxythiophen-2-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C=1SC=CC=1OC)N(CCO)C VDPVHNVRGBBVTG-UHFFFAOYSA-N 0.000 claims 2
- HAYILJUSPUGKGI-UHFFFAOYSA-N 2-[[2-cyclopropyl-8-fluoro-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound C1(CC1)C1=NC2=C(C=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCO)C)F HAYILJUSPUGKGI-UHFFFAOYSA-N 0.000 claims 2
- SIEJNOWZIDTSQJ-UHFFFAOYSA-N 2-[[4-(4-cyclohexylpiperidin-1-yl)-2-(1-fluorocyclopropyl)quinazolin-6-yl]-methylamino]ethanol Chemical compound C1(CCCCC1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCO)C)C1(CC1)F SIEJNOWZIDTSQJ-UHFFFAOYSA-N 0.000 claims 2
- TVMPWGASZCIMMZ-UHFFFAOYSA-N 2-[[4-[4-(2-methoxyphenyl)piperidin-1-yl]-2-(1-methylcyclopropyl)quinazolin-6-yl]-methylamino]ethanol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCO)C)C1(CC1)C TVMPWGASZCIMMZ-UHFFFAOYSA-N 0.000 claims 2
- RFRDMPKLPBPXEU-UHFFFAOYSA-N 2-[[4-[4-(2-methoxyphenyl)piperidin-1-yl]-2-[1-(trifluoromethyl)cyclopropyl]quinazolin-6-yl]-methylamino]ethanol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(C)CCO)C1(CC1)C(F)(F)F RFRDMPKLPBPXEU-UHFFFAOYSA-N 0.000 claims 2
- NEPBYKGTAIVOFI-UHFFFAOYSA-N 2-[[4-[4-[2-(dimethylamino)phenyl]piperidin-1-yl]-2-(1-fluorocyclobutyl)quinazolin-6-yl]-methylamino]ethanol Chemical compound CN(C1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCO)C)C1(CCC1)F)C NEPBYKGTAIVOFI-UHFFFAOYSA-N 0.000 claims 2
- HHAPARWQHIFMKW-UHFFFAOYSA-N 2-[[7-fluoro-2-(1-fluorocyclopropyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound COC1=CC=CC=C1C1CCN(CC1)C1=NC(=NC2=CC(F)=C(C=C12)N(C)CCO)C1(F)CC1 HHAPARWQHIFMKW-UHFFFAOYSA-N 0.000 claims 2
- JPWQBXUIRBWWIL-QFIPXVFZSA-N 2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]-6-[(3S)-3-methoxypyrrolidin-1-yl]quinazoline Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N1C[C@H](CC1)OC JPWQBXUIRBWWIL-QFIPXVFZSA-N 0.000 claims 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 2
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 201000009032 substance abuse Diseases 0.000 claims 2
- 231100000736 substance abuse Toxicity 0.000 claims 2
- 208000011117 substance-related disease Diseases 0.000 claims 2
- UNFCWKXOAHNNHK-HXUWFJFHSA-N (3R)-1-[2-(1-fluorocyclopropyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]pyrrolidin-3-ol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N1C[C@@H](CC1)O UNFCWKXOAHNNHK-HXUWFJFHSA-N 0.000 claims 1
- UNFCWKXOAHNNHK-FQEVSTJZSA-N (3S)-1-[2-(1-fluorocyclopropyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]pyrrolidin-3-ol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N1C[C@H](CC1)O UNFCWKXOAHNNHK-FQEVSTJZSA-N 0.000 claims 1
- INRBANSDBRGLRS-UHFFFAOYSA-N 1-[2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-N,N-dimethylpiperidin-4-amine Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N1CCC(CC1)N(C)C INRBANSDBRGLRS-UHFFFAOYSA-N 0.000 claims 1
- KQOJNRJDNGMXQW-UHFFFAOYSA-N 1-[2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]piperidin-4-ol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N1CCC(O)CC1)C1CC1 KQOJNRJDNGMXQW-UHFFFAOYSA-N 0.000 claims 1
- SQSASMLYFCBHPV-UHFFFAOYSA-N 1-[2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]pyrrolidin-3-ol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N1CCC(O)C1)C1CC1 SQSASMLYFCBHPV-UHFFFAOYSA-N 0.000 claims 1
- PUCQMUWGJKWMRI-UHFFFAOYSA-N 1-[8-chloro-2-(1-fluorocyclopropyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]pyrrolidin-3-ol Chemical compound ClC=1C=C(C=C2C(=NC(=NC=12)C1(CC1)F)N1CCC(CC1)C1=C(C=CC=C1)OC)N1CC(CC1)O PUCQMUWGJKWMRI-UHFFFAOYSA-N 0.000 claims 1
- MOJVGLAQYJKYQK-UHFFFAOYSA-N 2-(1-fluorocyclobutyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]-N-methyl-N-(2-morpholin-4-ylethyl)quinazolin-6-amine Chemical compound FC1(CCC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCN1CCOCC1)C MOJVGLAQYJKYQK-UHFFFAOYSA-N 0.000 claims 1
- VBZMXFCLNPYXGH-UHFFFAOYSA-N 2-(1-fluorocyclopropyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]-N-methyl-N-propylquinazolin-6-amine Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCC)C VBZMXFCLNPYXGH-UHFFFAOYSA-N 0.000 claims 1
- PUOWKWPAXWOGIH-UHFFFAOYSA-N 2-(1-fluorocyclopropyl)-N-(2-methoxyethyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]-N-methylquinazolin-6-amine Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(C)CCOC PUOWKWPAXWOGIH-UHFFFAOYSA-N 0.000 claims 1
- GNSJVEIUKZFLII-UHFFFAOYSA-N 2-(1-fluorocyclopropyl)-N-[2-(2-fluoroethoxy)ethyl]-4-[4-(2-methoxyphenyl)piperidin-1-yl]-N-methylquinazolin-6-amine Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(C)CCOCCF GNSJVEIUKZFLII-UHFFFAOYSA-N 0.000 claims 1
- RYUBYUHKYQBTMP-UHFFFAOYSA-N 2-N-cyclobutyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]-6-N-methyl-6-N-propylquinazoline-2,6-diamine Chemical compound C1(CCC1)NC1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCC)C RYUBYUHKYQBTMP-UHFFFAOYSA-N 0.000 claims 1
- ZSRGRQMMDDLRSB-UHFFFAOYSA-N 2-[4-[2-cyclopropyl-6-[methyl(2-morpholin-4-ylethyl)amino]quinazolin-4-yl]piperazin-1-yl]cyclopentan-1-ol Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCN(CC1)C1C(CCC1)O)N(CCN1CCOCC1)C ZSRGRQMMDDLRSB-UHFFFAOYSA-N 0.000 claims 1
- ZAPCFZAGTOOGFP-UHFFFAOYSA-N 2-[4-[2-cyclopropyl-6-[methyl(propyl)amino]quinazolin-4-yl]piperazin-1-yl]cyclopentan-1-ol Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCN(CC1)C1C(CCC1)O)N(CCC)C ZAPCFZAGTOOGFP-UHFFFAOYSA-N 0.000 claims 1
- DCSMIYHPFWSTAI-UHFFFAOYSA-N 2-[[2-(1-fluorocyclobutyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]pyrido[3,4-d]pyrimidin-6-yl]-methylamino]ethanol Chemical compound FC1(CCC1)C=1N=C(C2=C(N=1)C=NC(=C2)N(CCO)C)N1CCC(CC1)C1=C(C=CC=C1)OC DCSMIYHPFWSTAI-UHFFFAOYSA-N 0.000 claims 1
- PTGZYCCNOLGXNW-UHFFFAOYSA-N 2-[[2-(1-fluorocyclobutyl)-4-[4-(3-methoxypyrazin-2-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CCC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=NC=CN=C1OC)N(CCO)C PTGZYCCNOLGXNW-UHFFFAOYSA-N 0.000 claims 1
- VHBZAXNDJDJDBT-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopentyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CCCC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCO)C VHBZAXNDJDJDBT-UHFFFAOYSA-N 0.000 claims 1
- STCVZTQULCNRFV-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(2-methoxycyclohexyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1C(CCCC1)OC)N(CCO)C STCVZTQULCNRFV-UHFFFAOYSA-N 0.000 claims 1
- CGYAGEFRHONHQE-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]acetic acid Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CC(=O)O)C CGYAGEFRHONHQE-UHFFFAOYSA-N 0.000 claims 1
- IPBWPASLBVYBRX-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(2-methoxypyridin-3-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C=1C(=NC=CC=1)OC)N(CCO)C IPBWPASLBVYBRX-UHFFFAOYSA-N 0.000 claims 1
- MDXLNHPYSRIMBX-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(3-methoxypyrazin-2-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=NC=CN=C1OC)N(CCO)C MDXLNHPYSRIMBX-UHFFFAOYSA-N 0.000 claims 1
- RNTYDOJPGNZLAB-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(3-methoxypyridin-2-yl)piperazin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCN(CC1)C1=NC=CC=C1OC)N(CCO)C RNTYDOJPGNZLAB-UHFFFAOYSA-N 0.000 claims 1
- DWRNVKJPTZELIW-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(3-methoxypyridin-2-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=NC=CC=C1OC)N(CCO)C DWRNVKJPTZELIW-UHFFFAOYSA-N 0.000 claims 1
- AIJZUMVUKYYUQD-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(3-methoxypyridin-4-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=NC=C1)OC)N(CCO)C AIJZUMVUKYYUQD-UHFFFAOYSA-N 0.000 claims 1
- ITVDMACUSARXLN-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(4-iodo-2-methoxyphenyl)piperazin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCN(CC1)C1=C(C=C(C=C1)I)OC)N(CCO)C ITVDMACUSARXLN-UHFFFAOYSA-N 0.000 claims 1
- FWLPWNPXPAWKDY-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(4-methoxypyridin-3-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C=1C=NC=CC=1OC)N(CCO)C FWLPWNPXPAWKDY-UHFFFAOYSA-N 0.000 claims 1
- OXVOXIXQMSZKQM-UHFFFAOYSA-N 2-[[2-(1-fluorocyclopropyl)-4-[4-(5-methoxypyrimidin-4-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=NC=NC=C1OC)N(CCO)C OXVOXIXQMSZKQM-UHFFFAOYSA-N 0.000 claims 1
- QWZQBLFVZCIFRK-UHFFFAOYSA-N 2-[[2-(cyclobutylamino)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound C1(CCC1)NC1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCO)C QWZQBLFVZCIFRK-UHFFFAOYSA-N 0.000 claims 1
- PNDBFIFSSFFOIT-UHFFFAOYSA-N 2-[[2-[1-(fluoromethyl)cyclopropyl]-4-[4-(3-methoxypyrazin-2-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FCC1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=NC=CN=C1OC)N(CCO)C PNDBFIFSSFFOIT-UHFFFAOYSA-N 0.000 claims 1
- HODWJSJMXZRVHQ-UHFFFAOYSA-N 2-[[2-cyclopropyl-4-[4-(2-methoxycyclopentyl)piperazin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCN(CC1)C1C(CCC1)OC)N(CCO)C HODWJSJMXZRVHQ-UHFFFAOYSA-N 0.000 claims 1
- MBJDJOWCPZTZGV-UHFFFAOYSA-N 2-[[2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]-7-methylquinazolin-6-yl]-methylamino]ethanol Chemical compound C1(CC1)C1=NC2=CC(=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCO)C)C MBJDJOWCPZTZGV-UHFFFAOYSA-N 0.000 claims 1
- KJRIJBVRTOLCQH-UHFFFAOYSA-N 2-[[2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]-8-methylquinazolin-6-yl]-methylamino]ethanol Chemical compound C1(CC1)C1=NC2=C(C=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCO)C)C KJRIJBVRTOLCQH-UHFFFAOYSA-N 0.000 claims 1
- ARFBWKMJVLZODB-UHFFFAOYSA-N 2-[[2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]pyrido[3,4-d]pyrimidin-6-yl]-methylamino]ethanol Chemical compound C1(CC1)C=1N=C(C2=C(N=1)C=NC(=C2)N(CCO)C)N1CCC(CC1)C1=C(C=CC=C1)OC ARFBWKMJVLZODB-UHFFFAOYSA-N 0.000 claims 1
- CMRWUKHTTDUPBJ-UHFFFAOYSA-N 2-[[2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]acetic acid Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(C)CC(O)=O)C1CC1 CMRWUKHTTDUPBJ-UHFFFAOYSA-N 0.000 claims 1
- KRDPODVVQAPBRW-UHFFFAOYSA-N 2-[[2-cyclopropyl-4-[4-[2-(dimethylamino)phenyl]piperidin-1-yl]-7-fluoroquinazolin-6-yl]-methylamino]ethanol Chemical compound C1(CC1)C1=NC2=CC(=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)N(C)C)N(CCO)C)F KRDPODVVQAPBRW-UHFFFAOYSA-N 0.000 claims 1
- GLLCLDNXSXSRBM-UHFFFAOYSA-N 2-[[2-cyclopropyl-4-[6-(2-methoxyphenyl)-2,6-diazaspiro[3.3]heptan-2-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CC2(C1)CN(C2)C1=C(C=CC=C1)OC)N(CCO)C GLLCLDNXSXSRBM-UHFFFAOYSA-N 0.000 claims 1
- RJCHOKKXWPEPFN-UHFFFAOYSA-N 2-[[2-cyclopropyl-7-fluoro-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound C1(CC1)C1=NC2=CC(=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCO)C)F RJCHOKKXWPEPFN-UHFFFAOYSA-N 0.000 claims 1
- IYXHEPYZZHBMIL-UHFFFAOYSA-N 2-[[4-[4-(2-methoxyphenyl)piperidin-1-yl]-2-(1-methylcyclobutyl)quinazolin-6-yl]-methylamino]ethanol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCO)C)C1(CCC1)C IYXHEPYZZHBMIL-UHFFFAOYSA-N 0.000 claims 1
- CHWVPZCNJJMGBT-UHFFFAOYSA-N 2-[[4-[4-(2-methoxyphenyl)piperidin-1-yl]-2-(1-methylcyclopentyl)quinazolin-6-yl]-methylamino]ethanol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCO)C)C1(CCCC1)C CHWVPZCNJJMGBT-UHFFFAOYSA-N 0.000 claims 1
- ZGXBEBBPBRYREY-UHFFFAOYSA-N 2-[[4-[4-(2-methoxyphenyl)piperidin-1-yl]-2-[1-(trifluoromethyl)cyclobutyl]quinazolin-6-yl]-methylamino]ethanol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCO)C)C1(CCC1)C(F)(F)F ZGXBEBBPBRYREY-UHFFFAOYSA-N 0.000 claims 1
- IFCBNIBEMTYLNI-UHFFFAOYSA-N 2-[[4-[4-(2-methoxyphenyl)piperidin-1-yl]-2-[1-(trifluoromethyl)cyclopentyl]quinazolin-6-yl]-methylamino]ethanol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(C)CCO)C1(CCCC1)C(F)(F)F IFCBNIBEMTYLNI-UHFFFAOYSA-N 0.000 claims 1
- OPWVJCAAWCOHRB-UHFFFAOYSA-N 2-[[4-[4-(3-methoxypyrazin-2-yl)piperidin-1-yl]-2-(1-methylcyclopropyl)quinazolin-6-yl]-methylamino]ethanol Chemical compound COC=1C(=NC=CN=1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCO)C)C1(CC1)C OPWVJCAAWCOHRB-UHFFFAOYSA-N 0.000 claims 1
- IWFKQNHODMZNLI-UHFFFAOYSA-N 2-[[4-[4-[2-(azetidin-1-yl)phenyl]piperidin-1-yl]-2-(1-methylcyclopropyl)quinazolin-6-yl]-methylamino]ethanol Chemical compound N1(CCC1)C1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCO)C)C1(CC1)C IWFKQNHODMZNLI-UHFFFAOYSA-N 0.000 claims 1
- DHFCLVPOGFEGGU-UHFFFAOYSA-N 2-[[4-[4-[2-(dimethylamino)phenyl]piperidin-1-yl]-2-(1-fluorocyclopentyl)quinazolin-6-yl]-methylamino]ethanol Chemical compound CN(C)C1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(C)CCO)C1(F)CCCC1 DHFCLVPOGFEGGU-UHFFFAOYSA-N 0.000 claims 1
- AWMYQQQIHYNFSV-UHFFFAOYSA-N 2-[[4-[4-[2-(dimethylamino)phenyl]piperidin-1-yl]-2-(1-methylcyclopentyl)quinazolin-6-yl]-methylamino]ethanol Chemical compound CN(C)C1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(C)CCO)C1(C)CCCC1 AWMYQQQIHYNFSV-UHFFFAOYSA-N 0.000 claims 1
- ABKHBKAVXAXYNJ-UHFFFAOYSA-N 2-[[4-[4-[2-(dimethylamino)phenyl]piperidin-1-yl]-2-(1-methylcyclopropyl)quinazolin-6-yl]-methylamino]ethanol Chemical compound CN(C)C1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(C)CCO)C1(C)CC1 ABKHBKAVXAXYNJ-UHFFFAOYSA-N 0.000 claims 1
- PRMXDNMIOQBLJT-UHFFFAOYSA-N 2-[[4-[4-[2-(dimethylamino)phenyl]piperidin-1-yl]-2-[1-(trifluoromethyl)cyclobutyl]quinazolin-6-yl]-methylamino]ethanol Chemical compound CN(C1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCO)C)C1(CCC1)C(F)(F)F)C PRMXDNMIOQBLJT-UHFFFAOYSA-N 0.000 claims 1
- XHWPDJBOSAONHF-UHFFFAOYSA-N 2-[[4-[4-[2-(dimethylamino)phenyl]piperidin-1-yl]-2-[1-(trifluoromethyl)cyclopentyl]quinazolin-6-yl]-methylamino]ethanol Chemical compound CN(C1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCO)C)C1(CCCC1)C(F)(F)F)C XHWPDJBOSAONHF-UHFFFAOYSA-N 0.000 claims 1
- LZHJOPRARNCKCR-UHFFFAOYSA-N 2-[[4-[4-[2-(dimethylamino)phenyl]piperidin-1-yl]-2-[1-(trifluoromethyl)cyclopropyl]quinazolin-6-yl]-methylamino]ethanol Chemical compound CN(C1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCO)C)C1(CC1)C(F)(F)F)C LZHJOPRARNCKCR-UHFFFAOYSA-N 0.000 claims 1
- KZPWNDTVRVZKTA-UHFFFAOYSA-N 2-[[5-chloro-2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(N(C)CCO)C(Cl)=C12)C1CC1 KZPWNDTVRVZKTA-UHFFFAOYSA-N 0.000 claims 1
- ZQFKQUHAUGTZMZ-UHFFFAOYSA-N 2-[[8-chloro-2-(1-fluorocyclobutyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound ClC=1C=C(C=C2C(=NC(=NC=12)C1(CCC1)F)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCO)C ZQFKQUHAUGTZMZ-UHFFFAOYSA-N 0.000 claims 1
- NBDWICHDWMEPRR-UHFFFAOYSA-N 2-[[8-chloro-2-(1-fluorocyclopropyl)-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound ClC=1C=C(C=C2C(=NC(=NC=12)C1(CC1)F)N1CCC(CC1)C1=C(C=CC=C1)OC)N(CCO)C NBDWICHDWMEPRR-UHFFFAOYSA-N 0.000 claims 1
- ANBQSYOMPVETOT-UHFFFAOYSA-N 2-[[8-chloro-2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=C(Cl)C=C(C=C12)N(C)CCO)C1CC1 ANBQSYOMPVETOT-UHFFFAOYSA-N 0.000 claims 1
- MMSMYIOENCOVEB-UHFFFAOYSA-N 2-[[8-fluoro-2-(1-fluorocyclopropyl)-4-[4-(2-methoxypyridin-3-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC=1C=C(C=C2C(=NC(=NC=12)C1(CC1)F)N1CCC(CC1)C=1C(=NC=CC=1)OC)N(CCO)C MMSMYIOENCOVEB-UHFFFAOYSA-N 0.000 claims 1
- SSLJPKXWVAGMPD-UHFFFAOYSA-N 2-[[8-fluoro-2-(1-fluorocyclopropyl)-4-[4-(3-methoxypyrazin-2-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC=1C=C(C=C2C(=NC(=NC=12)C1(CC1)F)N1CCC(CC1)C1=NC=CN=C1OC)N(CCO)C SSLJPKXWVAGMPD-UHFFFAOYSA-N 0.000 claims 1
- RIIPYMOLSPWUCW-UHFFFAOYSA-N 2-[[8-fluoro-2-(1-fluorocyclopropyl)-4-[4-(3-methoxypyridin-2-yl)piperazin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC=1C=C(C=C2C(=NC(=NC=12)C1(CC1)F)N1CCN(CC1)C1=NC=CC=C1OC)N(CCO)C RIIPYMOLSPWUCW-UHFFFAOYSA-N 0.000 claims 1
- WVYWIROOPGNCKO-UHFFFAOYSA-N 2-[[8-fluoro-2-(1-fluorocyclopropyl)-4-[4-(3-methoxypyridin-2-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC=1C=C(C=C2C(=NC(=NC=12)C1(CC1)F)N1CCC(CC1)C1=NC=CC=C1OC)N(CCO)C WVYWIROOPGNCKO-UHFFFAOYSA-N 0.000 claims 1
- QTKUDCGLSDKKHF-UHFFFAOYSA-N 2-[[8-fluoro-2-(1-fluorocyclopropyl)-4-[4-(5-methoxypyrimidin-4-yl)piperidin-1-yl]quinazolin-6-yl]-methylamino]ethanol Chemical compound FC=1C=C(C=C2C(=NC(=NC=12)C1(CC1)F)N1CCC(CC1)C1=NC=NC=C1OC)N(CCO)C QTKUDCGLSDKKHF-UHFFFAOYSA-N 0.000 claims 1
- VLJIIIOCWBYIQC-UHFFFAOYSA-N 2-[[8-fluoro-4-[4-(3-methoxypyrazin-2-yl)piperidin-1-yl]-2-(1-methylcyclopropyl)quinazolin-6-yl]-methylamino]ethanol Chemical compound FC=1C=C(C=C2C(=NC(=NC=12)C1(CC1)C)N1CCC(CC1)C1=NC=CN=C1OC)N(CCO)C VLJIIIOCWBYIQC-UHFFFAOYSA-N 0.000 claims 1
- AWSDFFYJPSLCOG-UHFFFAOYSA-N 2-cyclopropyl-4-[4-(2-methoxycyclopentyl)piperazin-1-yl]-N-methyl-N-propylquinazolin-6-amine Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCN(CC1)C1C(CCC1)OC)N(CCC)C AWSDFFYJPSLCOG-UHFFFAOYSA-N 0.000 claims 1
- JPWQBXUIRBWWIL-UHFFFAOYSA-N 2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]-6-(3-methoxypyrrolidin-1-yl)quinazoline Chemical compound C1(CC1)C1=NC2=CC=C(C=C2C(=N1)N1CCC(CC1)C1=C(C=CC=C1)OC)N1CC(CC1)OC JPWQBXUIRBWWIL-UHFFFAOYSA-N 0.000 claims 1
- OYPGNTLBOHWGNH-UHFFFAOYSA-N 2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]-6-(4-methoxypiperidin-1-yl)quinazoline Chemical compound COC1CCN(CC1)C1=CC=C2N=C(N=C(N3CCC(CC3)C3=C(OC)C=CC=C3)C2=C1)C1CC1 OYPGNTLBOHWGNH-UHFFFAOYSA-N 0.000 claims 1
- 125000004791 2-fluoroethoxy group Chemical group FCCO* 0.000 claims 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
- VVXGYDAETLSKKU-UHFFFAOYSA-N 4-[4-(2-methoxyphenyl)piperidin-1-yl]-2-N,2-N,6-N-trimethyl-6-N-propylquinazoline-2,6-diamine Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCC)C)N(C)C VVXGYDAETLSKKU-UHFFFAOYSA-N 0.000 claims 1
- BPTJOYQPMTZTSA-UHFFFAOYSA-N 4-[4-(2-methoxyphenyl)piperidin-1-yl]-2-N,2-N-dimethyl-6-N,6-N-dipropylquinazoline-2,6-diamine Chemical compound COC1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(CCC)CCC)N(C)C BPTJOYQPMTZTSA-UHFFFAOYSA-N 0.000 claims 1
- RHOCAWMHTLRULS-UHFFFAOYSA-N 4-[4-(2-methoxyphenyl)piperidin-1-yl]-N-methyl-2-[1-[methyl(propyl)amino]cyclopropyl]-N-propylquinazolin-6-amine Chemical compound CCCN(C)C1=CC=C2N=C(N=C(N3CCC(CC3)C3=C(OC)C=CC=C3)C2=C1)C1(CC1)N(C)CCC RHOCAWMHTLRULS-UHFFFAOYSA-N 0.000 claims 1
- SBRPEWYFVNYVFK-UHFFFAOYSA-N 4-[4-[2-(azetidin-1-yl)phenyl]piperidin-1-yl]-N-(2-methoxyethyl)-N-methyl-2-(1-methylcyclopropyl)quinazolin-6-amine Chemical compound N1(CCC1)C1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(C)CCOC)C1(CC1)C SBRPEWYFVNYVFK-UHFFFAOYSA-N 0.000 claims 1
- WCTGUAOEHQPXLV-UHFFFAOYSA-N 4-[4-[2-(dimethylamino)phenyl]piperidin-1-yl]-N-(2-methoxyethyl)-N-methyl-2-(1-methylcyclopropyl)quinazolin-6-amine Chemical class CN(C1=C(C=CC=C1)C1CCN(CC1)C1=NC(=NC2=CC=C(C=C12)N(C)CCOC)C1(CC1)C)C WCTGUAOEHQPXLV-UHFFFAOYSA-N 0.000 claims 1
- 101000591385 Homo sapiens Neurotensin receptor type 1 Proteins 0.000 claims 1
- RGWFVVKSJUSKTE-UHFFFAOYSA-N N-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-4-(1,3-thiazol-4-yl)benzamide Chemical group COC1=CC=CC=C1N1CCN(CCCCNC(=O)C=2C=CC(=CC=2)C=2N=CSC=2)CC1 RGWFVVKSJUSKTE-UHFFFAOYSA-N 0.000 claims 1
- 208000012902 Nervous system disease Diseases 0.000 claims 1
- 102000050267 Neurotensin Human genes 0.000 claims 1
- 101800001814 Neurotensin Proteins 0.000 claims 1
- 102100033986 Neurotensin receptor type 1 Human genes 0.000 claims 1
- 125000004450 alkenylene group Chemical group 0.000 claims 1
- 125000004419 alkynylene group Chemical group 0.000 claims 1
- 125000006580 bicyclic heterocycloalkyl group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- KTHXBEHDVMTNOH-UHFFFAOYSA-N cyclobutanol Chemical compound OC1CCC1 KTHXBEHDVMTNOH-UHFFFAOYSA-N 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- YXWNCNXDAUTGQB-UHFFFAOYSA-N ethyl 2-[[1-[2-cyclopropyl-4-[4-(2-methoxyphenyl)piperidin-1-yl]quinazolin-6-yl]piperidin-4-yl]-methylamino]acetate Chemical compound C(C)OC(CN(C)C1CCN(CC1)C=1C=C2C(=NC(=NC2=CC=1)C1CC1)N1CCC(CC1)C1=C(C=CC=C1)OC)=O YXWNCNXDAUTGQB-UHFFFAOYSA-N 0.000 claims 1
- 125000004428 fluoroalkoxy group Chemical group 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- 125000006578 monocyclic heterocycloalkyl group Chemical group 0.000 claims 1
- 230000004770 neurodegeneration Effects 0.000 claims 1
- 208000015122 neurodegenerative disease Diseases 0.000 claims 1
- PCJGZPGTCUMMOT-ISULXFBGSA-N neurotensin Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(O)=O)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H]1NC(=O)CC1)C1=CC=C(O)C=C1 PCJGZPGTCUMMOT-ISULXFBGSA-N 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462017046P | 2014-06-25 | 2014-06-25 | |
| US62/017,046 | 2014-06-25 | ||
| PCT/US2015/037515 WO2015200534A2 (en) | 2014-06-25 | 2015-06-24 | Small molecule agonists of neurotensin receptor 1 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017519772A JP2017519772A (ja) | 2017-07-20 |
| JP2017519772A5 true JP2017519772A5 (enExample) | 2018-08-09 |
| JP6599908B2 JP6599908B2 (ja) | 2019-10-30 |
Family
ID=54938931
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016574242A Active JP6599908B2 (ja) | 2014-06-25 | 2015-06-24 | ニューロテンシン受容体1の小分子アゴニスト |
Country Status (5)
| Country | Link |
|---|---|
| US (3) | US10118902B2 (enExample) |
| EP (1) | EP3160961B1 (enExample) |
| JP (1) | JP6599908B2 (enExample) |
| CA (1) | CA2952732C (enExample) |
| WO (1) | WO2015200534A2 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004011217B4 (de) | 2004-03-04 | 2006-11-30 | Dr. Osypka Gmbh | Vorrichtung zum Implantieren einer Herzschrittmacher - und/oder Defibrillations-Elektrode |
| EP2938608B1 (en) | 2012-12-20 | 2021-08-04 | Sanford-Burnham Medical Research Institute | Small molecule agonists of neurotensin receptor 1 |
| JP6599908B2 (ja) * | 2014-06-25 | 2019-10-30 | サンフォード−バーンハム メディカル リサーチ インスティテュート | ニューロテンシン受容体1の小分子アゴニスト |
| CN109641886B (zh) * | 2015-11-25 | 2022-11-18 | 康威基内有限公司 | 双环bet布罗莫结构域抑制剂及其用途 |
| CN107903209B (zh) * | 2017-12-29 | 2021-05-14 | 宁夏忠同生物科技有限公司 | 一种2-氨基-5-氟吡啶-3-甲酸甲酯的合成方法 |
| CN109251196B (zh) * | 2018-01-24 | 2020-11-13 | 浙江工业大学 | 氨基苯并[d]氮杂*基喹唑啉类化合物及其制备方法和应用 |
| WO2022076285A1 (en) * | 2020-10-06 | 2022-04-14 | D.E. Shaw Research, Llc | LACTAM COMPOUNDS AS Kv1.3 POTASSIUM SHAKER CHANNEL BLOCKERS |
| US20240398806A1 (en) * | 2021-05-13 | 2024-12-05 | Duke University | Compositions For and Methods of Treating and/or Preventing Pain |
| US12091454B2 (en) | 2022-12-28 | 2024-09-17 | Development Center For Biotechnology | Humanized anti-human neurotensin receptor 1 antibodies and their uses |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58172379A (ja) | 1982-04-02 | 1983-10-11 | Showa Denko Kk | 新規なキナゾリン誘導体 |
| CA2118117A1 (en) | 1993-02-18 | 1994-08-19 | Shigeki Fujiwara | Adenosine uptake inhibitor |
| US5866562A (en) | 1996-10-25 | 1999-02-02 | Bayer Aktiengesellschaft | Ring-bridged bis-quinolines |
| JP2004509876A (ja) | 2000-09-20 | 2004-04-02 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフトング | 4−アミノ−キナゾリン |
| US7713983B2 (en) | 2003-03-03 | 2010-05-11 | Vertex Pharmaceuticals Incorporated | Quinazolines useful as modulators of ion channels |
| MXPA06005019A (es) * | 2003-11-03 | 2006-07-06 | Warner Lambert Co | Nuevos inhibidores de la recaptacion de norpinefrina para el tratamiento de transtornos del sistema nervioso central. |
| WO2006007864A1 (en) | 2004-07-17 | 2006-01-26 | Max Planck Geselllschaft Zur Förderung Der Wissenschaft | Treating neurodegenerative conditions |
| AU2006329202A1 (en) | 2005-12-21 | 2007-06-28 | Painceptor Pharma Corporation | Compositions and methods for modulating gated ion channels |
| US8153803B2 (en) | 2006-07-18 | 2012-04-10 | The General Hospital Corporation | Compositions and methods for modulating sirtuin activity |
| CA2709784A1 (en) | 2007-12-21 | 2009-07-09 | University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| WO2011153553A2 (en) * | 2010-06-04 | 2011-12-08 | The Regents Of The University Of California | Methods and compositions for kinase inhibition |
| CN102786483B (zh) | 2011-05-19 | 2016-03-30 | 复旦大学 | 4-(4-苯基哌嗪基)喹唑啉类衍生物的药用用途 |
| NZ706857A (en) * | 2012-09-28 | 2018-05-25 | Ignyta Inc | Azaquinazoline inhibitors of atypical protein kinase c |
| EP2938608B1 (en) | 2012-12-20 | 2021-08-04 | Sanford-Burnham Medical Research Institute | Small molecule agonists of neurotensin receptor 1 |
| JP6599908B2 (ja) | 2014-06-25 | 2019-10-30 | サンフォード−バーンハム メディカル リサーチ インスティテュート | ニューロテンシン受容体1の小分子アゴニスト |
-
2015
- 2015-06-24 JP JP2016574242A patent/JP6599908B2/ja active Active
- 2015-06-24 CA CA2952732A patent/CA2952732C/en active Active
- 2015-06-24 EP EP15811366.2A patent/EP3160961B1/en active Active
- 2015-06-24 WO PCT/US2015/037515 patent/WO2015200534A2/en not_active Ceased
- 2015-06-24 US US15/319,329 patent/US10118902B2/en active Active
-
2018
- 2018-09-24 US US16/140,363 patent/US10584103B2/en active Active
-
2020
- 2020-01-14 US US16/742,431 patent/US11261164B2/en active Active