WO2017173960A1 - Macro-hétérocycle utilisé pour supprimer le virus de l'hépatite c, sa préparation et son application - Google Patents
Macro-hétérocycle utilisé pour supprimer le virus de l'hépatite c, sa préparation et son application Download PDFInfo
- Publication number
- WO2017173960A1 WO2017173960A1 PCT/CN2017/079087 CN2017079087W WO2017173960A1 WO 2017173960 A1 WO2017173960 A1 WO 2017173960A1 CN 2017079087 W CN2017079087 W CN 2017079087W WO 2017173960 A1 WO2017173960 A1 WO 2017173960A1
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- 0 C*[C@](C1)(C1C1CC1)C(NS(C1CC1)(=O)=O)=O Chemical compound C*[C@](C1)(C1C1CC1)C(NS(C1CC1)(=O)=O)=O 0.000 description 3
- JYVONUVZMCXNRT-APWZRJJASA-N CC(C)(C)OC(N(C[C@@H](C1)Oc2nc(cc3OCOc3c3)c3nc2-c2cc(Br)ccc2)[C@@H]1C(OC)=O)=O Chemical compound CC(C)(C)OC(N(C[C@@H](C1)Oc2nc(cc3OCOc3c3)c3nc2-c2cc(Br)ccc2)[C@@H]1C(OC)=O)=O JYVONUVZMCXNRT-APWZRJJASA-N 0.000 description 1
- ZRCBLAXWEWVBIA-LESKNEHBSA-N CC(C)(C)OC(N[C@](C1)(C1C1CC1)C(O)=O)=O Chemical compound CC(C)(C)OC(N[C@](C1)(C1C1CC1)C(O)=O)=O ZRCBLAXWEWVBIA-LESKNEHBSA-N 0.000 description 1
- CJIPRINZFQIAAG-XHDPSFHLSA-N CC(C)(C)OC(N[C@](C1)([C@@H]1C1CC1)C(NS(C1CC1)(=O)=O)=O)=O Chemical compound CC(C)(C)OC(N[C@](C1)([C@@H]1C1CC1)C(NS(C1CC1)(=O)=O)=O)=O CJIPRINZFQIAAG-XHDPSFHLSA-N 0.000 description 1
- YYICMYZQIIQZQZ-WNKZXDIESA-N CC(C)(C)[C@@H](C(N(CC(C1)[O-2]c2nc(cc3OCOc3c3)c3nc2-c2cc(Br)ccc2)[C@@H]1C(OC)=O)=O)NC(OC(C)(C)C)=O Chemical compound CC(C)(C)[C@@H](C(N(CC(C1)[O-2]c2nc(cc3OCOc3c3)c3nc2-c2cc(Br)ccc2)[C@@H]1C(OC)=O)=O)NC(OC(C)(C)C)=O YYICMYZQIIQZQZ-WNKZXDIESA-N 0.000 description 1
- IURPJCHJZNSKII-GTDKFSSFSA-N CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)NC(OCC(C)(C)COc1cccc(-c2cc(ccc3c4OCO3)c4nc2OC)c1)=O Chemical compound CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)NC(OCC(C)(C)COc1cccc(-c2cc(ccc3c4OCO3)c4nc2OC)c1)=O IURPJCHJZNSKII-GTDKFSSFSA-N 0.000 description 1
- WFHVPOTYKBXIHO-WNCULLNHSA-N CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(O)=O)=O)NC(OCC(C)(C)COc1cc(-c2cc(ccc3c4OCO3)c4nc2O)ccc1)=O Chemical compound CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(O)=O)=O)NC(OCC(C)(C)COc1cc(-c2cc(ccc3c4OCO3)c4nc2O)ccc1)=O WFHVPOTYKBXIHO-WNCULLNHSA-N 0.000 description 1
- XOOORFYNBKDZOI-BKMJKUGQSA-N CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(O)=O)=O)NC(OCC(C)(C)COc1cccc(-c2nc(cc3OCOc3c3)c3nc2O)c1)=O Chemical compound CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(O)=O)=O)NC(OCC(C)(C)COc1cccc(-c2nc(cc3OCOc3c3)c3nc2O)c1)=O XOOORFYNBKDZOI-BKMJKUGQSA-N 0.000 description 1
- XNRMYYQGSGJVHP-WNCULLNHSA-N CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(OC)=O)=O)NC(OCC(C)(C)COc1cc(-c2nc(cc3OCOc3c3)c3nc2O)ccc1)=O Chemical compound CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(OC)=O)=O)NC(OCC(C)(C)COc1cc(-c2nc(cc3OCOc3c3)c3nc2O)ccc1)=O XNRMYYQGSGJVHP-WNCULLNHSA-N 0.000 description 1
- QSZPSGDZKKLUBB-OKOXAELESA-N CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2nc(c(O3)c(cc4)OC3(C)[O]=S(C3CC3)(NC([C@@H](CC3CC3)N3)=O)=O)c4nc2-c2cccc(OCC(C)(C)CO4)c2)[C@@H]1C3=O)=O)NC4=O Chemical compound CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2nc(c(O3)c(cc4)OC3(C)[O]=S(C3CC3)(NC([C@@H](CC3CC3)N3)=O)=O)c4nc2-c2cccc(OCC(C)(C)CO4)c2)[C@@H]1C3=O)=O)NC4=O QSZPSGDZKKLUBB-OKOXAELESA-N 0.000 description 1
- CHDYMWDXZBDFEP-SBQVMTCPSA-N CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2nc(c3c(cc4)OC(C)(C)O3)c4nc2-c2cc(OCC(C)(C)CO3)ccc2)[C@@H]1C(O)=O)=O)NC3=O Chemical compound CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2nc(c3c(cc4)OC(C)(C)O3)c4nc2-c2cc(OCC(C)(C)CO3)ccc2)[C@@H]1C(O)=O)=O)NC3=O CHDYMWDXZBDFEP-SBQVMTCPSA-N 0.000 description 1
- LRFZIPCTFBPFLX-SSDOTTSWSA-N CC(C)(C)[C@@H](C(O)=O)NC(OC(C)(C)C)=O Chemical compound CC(C)(C)[C@@H](C(O)=O)NC(OC(C)(C)C)=O LRFZIPCTFBPFLX-SSDOTTSWSA-N 0.000 description 1
- FWUIJRRFPBZQQT-UHFFFAOYSA-N CC(C)=[O]=S(C1CC1)(N)=O Chemical compound CC(C)=[O]=S(C1CC1)(N)=O FWUIJRRFPBZQQT-UHFFFAOYSA-N 0.000 description 1
- MUWAMLYKLZSGPE-NOZJJQNGSA-N CCOC([C@@](C1)([C@@H]1C=C)NC(OC(C)(C)C)=O)=O Chemical compound CCOC([C@@](C1)([C@@H]1C=C)NC(OC(C)(C)C)=O)=O MUWAMLYKLZSGPE-NOZJJQNGSA-N 0.000 description 1
- CRUOKPRFLOTHEQ-SNVBAGLBSA-N N[C@@]1(C(NS(C2CC2)(=O)=O)=O)C(C2CC2)=C1 Chemical compound N[C@@]1(C(NS(C2CC2)(=O)=O)=O)C(C2CC2)=C1 CRUOKPRFLOTHEQ-SNVBAGLBSA-N 0.000 description 1
- WZXFIDXRXIOGTR-UHFFFAOYSA-N Nc1ccc2OCOc2c1N Chemical compound Nc1ccc2OCOc2c1N WZXFIDXRXIOGTR-UHFFFAOYSA-N 0.000 description 1
- LQKCQACFVUTFIG-UHFFFAOYSA-N Oc1c(-c2cc(Br)ccc2)nc(c2c(cc3)OCO2)c3n1 Chemical compound Oc1c(-c2cc(Br)ccc2)nc(c2c(cc3)OCO2)c3n1 LQKCQACFVUTFIG-UHFFFAOYSA-N 0.000 description 1
- YCIMNLLNPGFGHC-UHFFFAOYSA-N Oc1ccccc1O Chemical compound Oc1ccccc1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 1
- YHKWFDPEASWKFQ-UHFFFAOYSA-N [O-][N+](c(cccc1O)c1O)=O Chemical compound [O-][N+](c(cccc1O)c1O)=O YHKWFDPEASWKFQ-UHFFFAOYSA-N 0.000 description 1
- PAHDCKCVXHLYQB-UHFFFAOYSA-N [O-][N+](c1ccc2OCOc2c1[N+]([O-])=O)=O Chemical compound [O-][N+](c1ccc2OCOc2c1[N+]([O-])=O)=O PAHDCKCVXHLYQB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/0808—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/056—Ortho-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
L'invention concerne un composé permettant de supprimer le virus de l'hépatite C (VHC), un procédé de préparation et une application pharmaceutique du composé. Le composé est représenté par la formule A. Divers substituants sont tels que définis dans la description.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201780000221.0A CN107074876B (zh) | 2016-04-08 | 2017-03-31 | 一类抑制丙肝病毒的大环状杂环化合物及其制备和用途 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610219170.8 | 2016-04-08 | ||
CN201610219170.8A CN107266529A (zh) | 2016-04-08 | 2016-04-08 | 一类抑制丙肝病毒的大环状杂环化合物及其制备和用途 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2017173960A1 true WO2017173960A1 (fr) | 2017-10-12 |
Family
ID=60000836
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CN2017/079087 WO2017173960A1 (fr) | 2016-04-08 | 2017-03-31 | Macro-hétérocycle utilisé pour supprimer le virus de l'hépatite c, sa préparation et son application |
Country Status (2)
Country | Link |
---|---|
CN (1) | CN107266529A (fr) |
WO (1) | WO2017173960A1 (fr) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107074876B (zh) * | 2016-04-08 | 2019-12-20 | 上海长森药业有限公司 | 一类抑制丙肝病毒的大环状杂环化合物及其制备和用途 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009134987A1 (fr) * | 2008-04-30 | 2009-11-05 | Enanta Pharmaceuticals, Inc. | Composés macrocycliques contenant du difluorométhyle comme inhibiteurs du virus de l’hépatite c |
CN101909446A (zh) * | 2007-11-14 | 2010-12-08 | 益安药业 | 作为丙型肝炎病毒抑制剂的含喹喔啉的化合物 |
WO2011049908A2 (fr) * | 2009-10-19 | 2011-04-28 | Enanta Pharmaceuticals, Inc. | Composés bismacrocycliques à titre d'inhibiteurs du virus de l'hépatite c |
CN102458444A (zh) * | 2009-05-13 | 2012-05-16 | 英安塔制药有限公司 | 用作丙型肝炎病毒抑制剂的大环化合物 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2011209051B2 (en) * | 2010-01-27 | 2015-01-15 | AB Pharma Ltd. | Polyheterocyclic compounds highly potent as HCV inhibitors |
CN111116563B (zh) * | 2013-06-06 | 2023-07-04 | 上海爱博医药科技有限公司 | 抑制丙肝病毒的化合物、药物组合物及其应用 |
-
2016
- 2016-04-08 CN CN201610219170.8A patent/CN107266529A/zh not_active Withdrawn
-
2017
- 2017-03-31 WO PCT/CN2017/079087 patent/WO2017173960A1/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101909446A (zh) * | 2007-11-14 | 2010-12-08 | 益安药业 | 作为丙型肝炎病毒抑制剂的含喹喔啉的化合物 |
WO2009134987A1 (fr) * | 2008-04-30 | 2009-11-05 | Enanta Pharmaceuticals, Inc. | Composés macrocycliques contenant du difluorométhyle comme inhibiteurs du virus de l’hépatite c |
CN102458444A (zh) * | 2009-05-13 | 2012-05-16 | 英安塔制药有限公司 | 用作丙型肝炎病毒抑制剂的大环化合物 |
WO2011049908A2 (fr) * | 2009-10-19 | 2011-04-28 | Enanta Pharmaceuticals, Inc. | Composés bismacrocycliques à titre d'inhibiteurs du virus de l'hépatite c |
Also Published As
Publication number | Publication date |
---|---|
CN107266529A (zh) | 2017-10-20 |
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