CA3029630A1 - Biarylmethyl heterocycles - Google Patents
Biarylmethyl heterocycles Download PDFInfo
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- CA3029630A1 CA3029630A1 CA3029630A CA3029630A CA3029630A1 CA 3029630 A1 CA3029630 A1 CA 3029630A1 CA 3029630 A CA3029630 A CA 3029630A CA 3029630 A CA3029630 A CA 3029630A CA 3029630 A1 CA3029630 A1 CA 3029630A1
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- Prior art keywords
- alkyl
- cycloalkyl
- haloalkyl
- hydroxyalkyl
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- 0 CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC1OC1CO*)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC1OC1CO*)(=O)=O 0.000 description 3
- IVCQHSXQUGAWAZ-UHFFFAOYSA-N CCCCCC(NS(c(ccc(CN1CCCC1)c1)c1-c1ccc(C[n]2c3nc(C)cc(C)c3nc2CC)cc1)(=O)=O)=O Chemical compound CCCCCC(NS(c(ccc(CN1CCCC1)c1)c1-c1ccc(C[n]2c3nc(C)cc(C)c3nc2CC)cc1)(=O)=O)=O IVCQHSXQUGAWAZ-UHFFFAOYSA-N 0.000 description 1
- NXVWCYUJVUSWCD-UHFFFAOYSA-N CCc1nc(c(C)cc(C)c2)c2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(c1cccc(-c(cc2C)cc3c2nc(CC)[n]3Cc(cc2)ccc2-c(cc(Cc2ccccc2)[s]2)c2S(NC(c2ccccc2)=O)(=O)=O)c1)=O)(=O)=O Chemical compound CCc1nc(c(C)cc(C)c2)c2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(c1cccc(-c(cc2C)cc3c2nc(CC)[n]3Cc(cc2)ccc2-c(cc(Cc2ccccc2)[s]2)c2S(NC(c2ccccc2)=O)(=O)=O)c1)=O)(=O)=O NXVWCYUJVUSWCD-UHFFFAOYSA-N 0.000 description 1
- HXZIRMOMABVAND-UHFFFAOYSA-N CCc1nc2c(C)cc(C(N(C)C)=O)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC1OC1c1ccccc1)(=O)=O Chemical compound CCc1nc2c(C)cc(C(N(C)C)=O)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC1OC1c1ccccc1)(=O)=O HXZIRMOMABVAND-UHFFFAOYSA-N 0.000 description 1
- BJXFTPUVBSFEOV-UHFFFAOYSA-N CCc1nc2c(C)cc(C)cc2[n]1Cc(cc1)ccc1C(CC(C)(CN1CCOCC1)S1)=C1S(NC(C(c1ccccc1)C1=CCC(C)C(Cc(cc2C)cc3c2nc(CC)[n]3Cc(cc2)ccc2-c(cc(Cc2ccccc2)[s]2)c2S(NC(c2ccccc2)=O)(=O)=O)=C1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)cc2[n]1Cc(cc1)ccc1C(CC(C)(CN1CCOCC1)S1)=C1S(NC(C(c1ccccc1)C1=CCC(C)C(Cc(cc2C)cc3c2nc(CC)[n]3Cc(cc2)ccc2-c(cc(Cc2ccccc2)[s]2)c2S(NC(c2ccccc2)=O)(=O)=O)=C1)=O)(=O)=O BJXFTPUVBSFEOV-UHFFFAOYSA-N 0.000 description 1
- CCJGLSZNKAYAAD-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(CCc1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(CCc1ccccc1)=O)(=O)=O CCJGLSZNKAYAAD-UHFFFAOYSA-N 0.000 description 1
- VUGNWEUFBXVLPS-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(c(cccc1)c1Oc1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(c(cccc1)c1Oc1ccccc1)=O)(=O)=O VUGNWEUFBXVLPS-UHFFFAOYSA-N 0.000 description 1
- XBPDOYQLLZWIGG-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(c1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(c1ccccc1)=O)(=O)=O XBPDOYQLLZWIGG-UHFFFAOYSA-N 0.000 description 1
- IMNRNJIVXFJTCL-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(Cc1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(Cc1ccccc1)=O)(=O)=O IMNRNJIVXFJTCL-UHFFFAOYSA-N 0.000 description 1
- QOUGSHMWCZQBOM-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O QOUGSHMWCZQBOM-UHFFFAOYSA-N 0.000 description 1
- SFJQWEVGLDUGLM-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(C1CC1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(C1CC1)=O)(=O)=O SFJQWEVGLDUGLM-UHFFFAOYSA-N 0.000 description 1
- OVYVZRZLFTWXDU-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O OVYVZRZLFTWXDU-UHFFFAOYSA-N 0.000 description 1
- MVDOITYZIMLXLE-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc1ccc(C(C)(C(C=C2)S(NC(c3cc(Cc(cc4C)nc5c4nc(CC)[n]5Cc(cc4)ccc4C(C(C)C(CN4CCOCC4)C=C4)=C4S(NC(c4ccccc4)=O)(=O)=O)ccc3)=O)(=O)=O)C=C2c2ccccc2)cc1 Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc1ccc(C(C)(C(C=C2)S(NC(c3cc(Cc(cc4C)nc5c4nc(CC)[n]5Cc(cc4)ccc4C(C(C)C(CN4CCOCC4)C=C4)=C4S(NC(c4ccccc4)=O)(=O)=O)ccc3)=O)(=O)=O)C=C2c2ccccc2)cc1 MVDOITYZIMLXLE-UHFFFAOYSA-N 0.000 description 1
- YFSODJRLDIOLRT-UHFFFAOYSA-N CCc1nc2c(C)ccnc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)ccnc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O YFSODJRLDIOLRT-UHFFFAOYSA-N 0.000 description 1
- AVFLSYMKOGBIER-UHFFFAOYSA-N CCc1nc2c(C)ccnc2[n]1Cc(cc1)ccc1-c1c(-c2n[nH]nn2)[s]c(Cc2ccccc2)c1 Chemical compound CCc1nc2c(C)ccnc2[n]1Cc(cc1)ccc1-c1c(-c2n[nH]nn2)[s]c(Cc2ccccc2)c1 AVFLSYMKOGBIER-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- A—HUMAN NECESSITIES
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4245—Oxadiazoles
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- A—HUMAN NECESSITIES
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- 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
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- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
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- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/26—Oxygen atoms
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- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/20—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
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- C—CHEMISTRY; METALLURGY
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- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
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- C—CHEMISTRY; METALLURGY
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- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
- C07D271/07—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
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- C07D401/00—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
- C07D401/02—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 two hetero rings
- C07D401/10—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 two hetero rings linked by a carbon chain containing aromatic rings
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- C07D403/10—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 carbon chain containing aromatic rings
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- 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
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
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- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
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- General Chemical & Material Sciences (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicinal Preparation (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Peptides Or Proteins (AREA)
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| CN109956870A (zh) * | 2017-12-14 | 2019-07-02 | 南京卡文迪许生物工程技术有限公司 | 一种罗沙司他的合成方法及其中间体化合物 |
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| EP4218934B1 (en) | 2018-10-05 | 2025-06-18 | Forma Therapeutics, Inc. | Inhibiting ubiquitin-specific protease 30 (usp30) |
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| KR102841588B1 (ko) * | 2019-06-20 | 2025-08-01 | 케모센트릭스, 인크. | Pd-l1 질환의 치료를 위한 화합물 |
| CN110479182A (zh) * | 2019-09-10 | 2019-11-22 | 肯特催化材料股份有限公司 | 一种多氨基双子表面活性剂及其制备方法与应用 |
| GB201913603D0 (en) | 2019-09-20 | 2019-11-06 | Vicore Pharma Ab | New compounds |
| GB202104033D0 (en) * | 2021-03-23 | 2021-05-05 | Vicore Pharma Ab | New compounds |
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| KR20240051999A (ko) * | 2021-08-26 | 2024-04-22 | 상하이 한서 바이오메디컬 컴퍼니 리미티드 | 방향족 고리 함유 생물학적 길항제, 이의 제조 방법 및 용도 |
| CN115321495B (zh) * | 2022-07-28 | 2023-07-21 | 东北石油大学 | 一种金属富氮化合物FeN8的合成方法 |
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2017
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- 2017-06-28 WO PCT/US2017/039646 patent/WO2018005591A1/en not_active Ceased
- 2017-06-28 AU AU2017289974A patent/AU2017289974B2/en not_active Ceased
- 2017-06-28 JP JP2018568791A patent/JP7231414B2/ja active Active
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- 2017-06-28 SG SG11201810837QA patent/SG11201810837QA/en unknown
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2018
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2022
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| KR20190025639A (ko) | 2019-03-11 |
| JP2019519586A (ja) | 2019-07-11 |
| MX2018015247A (es) | 2019-08-12 |
| ES2984389T3 (es) | 2024-10-29 |
| TW201811759A (zh) | 2018-04-01 |
| US12037324B2 (en) | 2024-07-16 |
| US11407733B2 (en) | 2022-08-09 |
| AR108906A1 (es) | 2018-10-10 |
| SG11201810837QA (en) | 2018-12-28 |
| JP7231414B2 (ja) | 2023-03-01 |
| KR102538999B1 (ko) | 2023-05-31 |
| EA201990159A1 (ru) | 2019-07-31 |
| US20190202808A1 (en) | 2019-07-04 |
| US20230045357A1 (en) | 2023-02-09 |
| IL263499B (en) | 2022-04-01 |
| AU2017289974A1 (en) | 2019-01-17 |
| EP3478672A1 (en) | 2019-05-08 |
| EA039493B1 (ru) | 2022-02-02 |
| CN109715615A (zh) | 2019-05-03 |
| EP3478672B1 (en) | 2024-04-10 |
| BR112018077075A2 (pt) | 2019-04-30 |
| WO2018005591A1 (en) | 2018-01-04 |
| IL263499A (en) | 2019-01-31 |
| AU2017289974B2 (en) | 2021-08-12 |
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