JP2020515516A5 - - Google Patents
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- JP2020515516A5 JP2020515516A5 JP2019537185A JP2019537185A JP2020515516A5 JP 2020515516 A5 JP2020515516 A5 JP 2020515516A5 JP 2019537185 A JP2019537185 A JP 2019537185A JP 2019537185 A JP2019537185 A JP 2019537185A JP 2020515516 A5 JP2020515516 A5 JP 2020515516A5
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- JP
- Japan
- Prior art keywords
- dihydro
- oxy
- chloro
- cyano
- ethoxy
- 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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- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 408
- 229940124530 sulfonamide Drugs 0.000 claims description 265
- 150000003456 sulfonamides Chemical class 0.000 claims description 262
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 215
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 153
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 140
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 134
- 239000004202 carbamide Substances 0.000 claims description 125
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 124
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 122
- 125000000623 heterocyclic group Chemical group 0.000 claims description 97
- -1 3-aminopiperidine-1-yl Chemical group 0.000 claims description 83
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 83
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims description 80
- 150000001875 compounds Chemical class 0.000 claims description 77
- 125000001072 heteroaryl group Chemical group 0.000 claims description 72
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 70
- 229910052757 nitrogen Inorganic materials 0.000 claims description 63
- 125000000217 alkyl group Chemical group 0.000 claims description 47
- 125000003118 aryl group Chemical group 0.000 claims description 43
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 43
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 40
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 39
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 38
- KZKRRZFCAYOXQE-UHFFFAOYSA-N 1$l^{2}-azinane Chemical group C1CC[N]CC1 KZKRRZFCAYOXQE-UHFFFAOYSA-N 0.000 claims description 36
- 229910052736 halogen Inorganic materials 0.000 claims description 36
- 150000002367 halogens Chemical class 0.000 claims description 36
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 34
- 229910052760 oxygen Inorganic materials 0.000 claims description 34
- 229910052717 sulfur Inorganic materials 0.000 claims description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims description 26
- 125000005842 heteroatom Chemical group 0.000 claims description 25
- 229910052698 phosphorus Inorganic materials 0.000 claims description 25
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 24
- 125000003114 inden-1-yl group Chemical group [H]C1=C([H])C([H])(*)C2=C([H])C([H])=C([H])C([H])=C12 0.000 claims description 21
- 229910052799 carbon Inorganic materials 0.000 claims description 20
- 125000003342 alkenyl group Chemical group 0.000 claims description 16
- 125000005647 linker group Chemical group 0.000 claims description 15
- YSERCIHBCXZJHY-HKUYNNGSSA-N (1S,2S)-6-chloro-2-(dimethylamino)-1-(2-methylphenoxy)-2,3-dihydro-1H-indene-4-carbonitrile Chemical compound ClC1=CC(=C2C[C@@H]([C@H](C2=C1)OC1=C(C=CC=C1)C)N(C)C)C#N YSERCIHBCXZJHY-HKUYNNGSSA-N 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 10
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 9
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 9
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 8
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound 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 8
- 125000001188 haloalkyl group Chemical group 0.000 claims description 8
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 8
- 125000003386 piperidinyl group Chemical group 0.000 claims description 7
- MGHNDJJPPOAIHK-UHFFFAOYSA-N 1H-inden-1-yl Chemical group C1=CC=C2[CH]C=CC2=C1 MGHNDJJPPOAIHK-UHFFFAOYSA-N 0.000 claims description 6
- 125000000304 alkynyl group Chemical group 0.000 claims description 6
- ZZLCFHIKESPLTH-UHFFFAOYSA-N 4-Methylbiphenyl Chemical compound C1=CC(C)=CC=C1C1=CC=CC=C1 ZZLCFHIKESPLTH-UHFFFAOYSA-N 0.000 claims description 4
- 208000002551 irritable bowel syndrome Diseases 0.000 claims description 4
- 125000004193 piperazinyl group Chemical group 0.000 claims description 4
- MMCSOJGCSIIZFZ-PMACEKPBSA-N ClC1=CC(=C2C[C@@H]([C@H](C2=C1)OC1=CC=C(C=C1)S(=O)(=O)N)N1CCNCC1)C#N Chemical compound ClC1=CC(=C2C[C@@H]([C@H](C2=C1)OC1=CC=C(C=C1)S(=O)(=O)N)N1CCNCC1)C#N MMCSOJGCSIIZFZ-PMACEKPBSA-N 0.000 claims description 3
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 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 3
- IQHXABCGSFAKPN-UHFFFAOYSA-N pyrrolidine-3-carboxamide Chemical compound NC(=O)C1CCNC1 IQHXABCGSFAKPN-UHFFFAOYSA-N 0.000 claims description 3
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 3
- HOAIIKMYWZFQAN-PMACEKPBSA-N (1S,2S)-6-chloro-1-phenoxy-2-piperazin-1-yl-2,3-dihydro-1H-indene-4-carbonitrile Chemical compound ClC1=CC(=C2C[C@@H]([C@H](C2=C1)OC1=CC=CC=C1)N1CCNCC1)C#N HOAIIKMYWZFQAN-PMACEKPBSA-N 0.000 claims description 2
- UDAUYRKMSQRJDG-BMUFGRPASA-N 1-[4-[6-[[(1S,2S)-6-chloro-4-cyano-2-piperazin-1-yl-2,3-dihydro-1H-inden-1-yl]oxy]-3,4-dihydro-1H-isoquinolin-2-yl]-4-oxobutyl]-3-[4-[[4-[6-[[(1S,2S)-6-chloro-4-cyano-2-piperazin-1-yl-2,3-dihydro-1H-inden-1-yl]oxy]-3,4-dihydro-1H-isoquinolin-2-yl]-4-oxobutyl]carbamoylamino]butyl]urea Chemical compound C(CCCNC(=O)NCCCC(N1CC2=CC=C(C=C2CC1)O[C@@H]1[C@H](CC2=C(C=C(C=C12)Cl)C#N)N1CCNCC1)=O)NC(=O)NCCCC(=O)N1CC2=CC=C(C=C2CC1)O[C@@H]1[C@H](CC2=C(C=C(C=C12)Cl)C#N)N1CCNCC1 UDAUYRKMSQRJDG-BMUFGRPASA-N 0.000 claims description 2
- DPBWFNDFMCCGGJ-UHFFFAOYSA-N 4-Piperidine carboxamide Chemical compound NC(=O)C1CCNCC1 DPBWFNDFMCCGGJ-UHFFFAOYSA-N 0.000 claims description 2
- STRWNSXHTGIOQH-SFTDATJTSA-N CC1=CC(C#N)=C(C[C@@H]([C@H]2OC(C=C3)=CC=C3S(N)(=O)=O)N3CCNCC3)C2=C1 Chemical compound CC1=CC(C#N)=C(C[C@@H]([C@H]2OC(C=C3)=CC=C3S(N)(=O)=O)N3CCNCC3)C2=C1 STRWNSXHTGIOQH-SFTDATJTSA-N 0.000 claims description 2
- RPLHIDLAYRDZBE-CZAAIQMYSA-N N[C@H]1CN(CCC1)[C@@H]1[C@H](C2=CC(=CC(=C2C1)C#N)Cl)OC1=CC=CC=C1 Chemical compound N[C@H]1CN(CCC1)[C@@H]1[C@H](C2=CC(=CC(=C2C1)C#N)Cl)OC1=CC=CC=C1 RPLHIDLAYRDZBE-CZAAIQMYSA-N 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims 8
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 8
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 3
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
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- 201000005991 hyperphosphatemia Diseases 0.000 claims 1
- 239000002694 phosphate binding agent Substances 0.000 claims 1
- 206010010774 Constipation Diseases 0.000 description 29
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 20
- 150000001345 alkine derivatives Chemical class 0.000 description 15
- PEDPVHYNSCOTLR-UAOJZALGSA-N (3R)-1-[(1S,2S)-4,6-dichloro-1-phenoxy-2,3-dihydro-1H-inden-2-yl]piperidin-3-amine Chemical compound N[C@H]1CN(CCC1)[C@@H]1[C@H](C2=CC(=CC(=C2C1)Cl)Cl)OC1=CC=CC=C1 PEDPVHYNSCOTLR-UAOJZALGSA-N 0.000 description 14
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-
2018
- 2018-01-09 CA CA3049678A patent/CA3049678A1/en active Pending
- 2018-01-09 JP JP2019537185A patent/JP7292207B2/ja active Active
- 2018-01-09 AU AU2018205400A patent/AU2018205400C1/en active Active
- 2018-01-09 CN CN202410183141.5A patent/CN118221656A/zh active Pending
- 2018-01-09 MX MX2019008170A patent/MX395405B/es unknown
- 2018-01-09 US US16/476,836 patent/US11242337B2/en active Active
- 2018-01-09 KR KR1020197023352A patent/KR102669987B1/ko active Active
- 2018-01-09 CN CN201880009820.3A patent/CN110267944B/zh active Active
- 2018-01-09 KR KR1020247017226A patent/KR20240090875A/ko active Pending
- 2018-01-09 UA UAA201908567A patent/UA126283C2/uk unknown
- 2018-01-09 EP EP18703655.3A patent/EP3565808B1/en active Active
- 2018-01-09 MA MA047207A patent/MA47207A/fr unknown
- 2018-01-09 WO PCT/US2018/013020 patent/WO2018129552A1/en not_active Ceased
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2019
- 2019-06-28 ZA ZA2019/04297A patent/ZA201904297B/en unknown
- 2019-07-02 IL IL267805A patent/IL267805B/en unknown
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2021
- 2021-12-21 US US17/558,227 patent/US20220306610A1/en not_active Abandoned
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2022
- 2022-08-02 AU AU2022211830A patent/AU2022211830A1/en not_active Abandoned
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2023
- 2023-01-04 JP JP2023000316A patent/JP2023052205A/ja not_active Withdrawn
- 2023-12-27 US US18/397,454 patent/US12281103B2/en active Active
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2025
- 2025-01-05 JP JP2025000028A patent/JP2025060986A/ja active Pending
- 2025-03-04 US US19/070,289 patent/US20250263401A1/en active Pending
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2026
- 2026-01-05 JP JP2026000533A patent/JP2026053715A/ja active Pending
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