CN115667238A - 一种五并五元环衍生物及其在医药上的应用 - Google Patents
一种五并五元环衍生物及其在医药上的应用 Download PDFInfo
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- CN115667238A CN115667238A CN202180036568.7A CN202180036568A CN115667238A CN 115667238 A CN115667238 A CN 115667238A CN 202180036568 A CN202180036568 A CN 202180036568A CN 115667238 A CN115667238 A CN 115667238A
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- KSIRAKMYTMKTDP-ZETCQYMHSA-N methyl 2-(bromomethyl)-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CBr)=N2)=C2S1)=O KSIRAKMYTMKTDP-ZETCQYMHSA-N 0.000 description 3
- XLLPAXJFQOFMRN-QMMMGPOBSA-N methyl 2-(bromomethyl)-1-[[(2S)-oxolan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCCC2)C(CBr)=N2)=C2S1)=O XLLPAXJFQOFMRN-QMMMGPOBSA-N 0.000 description 3
- XEIPUMDOWSHRGY-ZETCQYMHSA-N methyl 2-(chloromethyl)-3-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N=C(CCl)N2C[C@H]3OCC3)=C2S1)=O XEIPUMDOWSHRGY-ZETCQYMHSA-N 0.000 description 3
- CGYDCDUTOKPPEF-JTQLQIEISA-N methyl 2-[(4-bromo-2,5-difluorophenyl)methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CC(C=C(C(Br)=C2)F)=C2F)=N2)=C2S1)=O CGYDCDUTOKPPEF-JTQLQIEISA-N 0.000 description 3
- PYXMCWPHVSSWPP-LBPRGKRZSA-N methyl 2-[(4-bromo-2-fluoro-5-methylphenyl)methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound CC(C(Br)=C1)=CC(CC2=NC(SC(C(OC)=O)=C3)=C3N2C[C@H]2OCC2)=C1F PYXMCWPHVSSWPP-LBPRGKRZSA-N 0.000 description 3
- JQYPMMKHCLJCDP-GFCCVEGCSA-N methyl 2-[(4-bromo-2-fluorophenyl)methyl]-1-[[(2R)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@@H]2OCC2)C(CC(C=CC(Br)=C2)=C2F)=N2)=C2S1)=O JQYPMMKHCLJCDP-GFCCVEGCSA-N 0.000 description 3
- AYTGJNQYFYNNJV-ZDUSSCGKSA-N methyl 2-[(4-bromophenyl)methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CC(C=C2)=CC=C2Br)=N2)=C2S1)=O AYTGJNQYFYNNJV-ZDUSSCGKSA-N 0.000 description 3
- QUADJLFLGGFQGS-ZDUSSCGKSA-N methyl 2-[[4-(6-fluoropyridin-2-yl)-6-oxopyridazin-1-yl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CN2N=CC(C3=NC(F)=CC=C3)=CC2=O)=N2)=C2S1)=O QUADJLFLGGFQGS-ZDUSSCGKSA-N 0.000 description 3
- FBIRYEVDLYOTEV-QFIPXVFZSA-N methyl 2-[[4-[2-[(4-cyano-2-fluorophenyl)methoxy]pyridin-3-yl]piperidin-1-yl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CN(CC2)CCC2C2=CC=CN=C2OCC(C=CC(C#N)=C2)=C2F)=N2)=C2S1)=O FBIRYEVDLYOTEV-QFIPXVFZSA-N 0.000 description 3
- RYZPMHKEQCWSRP-NRFANRHFSA-N methyl 2-[[4-[6-[(4-cyano-2-fluorophenyl)methoxy]-5-fluoropyridin-2-yl]-2-fluorophenyl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CC(C=CC(C(C=C2)=NC(OCC(C=CC(C#N)=C3)=C3F)=C2F)=C2)=C2F)=N2)=C2S1)=O RYZPMHKEQCWSRP-NRFANRHFSA-N 0.000 description 3
- TXSUMEFPIKKKDW-NRFANRHFSA-N methyl 2-[[4-[6-[(4-cyano-2-fluorophenyl)methoxy]-5-fluoropyridin-2-yl]piperidin-1-yl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CN(CC2)CCC2C(C=C2)=NC(OCC(C=CC(C#N)=C3)=C3F)=C2F)=N2)=C2S1)=O TXSUMEFPIKKKDW-NRFANRHFSA-N 0.000 description 3
- GUHKZADYZMLJTB-QFIPXVFZSA-N methyl 2-[[4-[6-[(4-cyano-2-fluorophenyl)methoxy]pyridin-2-yl]-2-fluoro-5-methylphenyl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound CC(C(C1=NC(OCC(C=CC(C#N)=C2)=C2F)=CC=C1)=C1)=CC(CC2=NC(SC(C(OC)=O)=C3)=C3N2C[C@H]2OCC2)=C1F GUHKZADYZMLJTB-QFIPXVFZSA-N 0.000 description 3
- YQEMYYJRRCXBIF-NRFANRHFSA-N methyl 2-[[4-[6-[(4-cyano-2-fluorophenyl)methoxy]pyridin-2-yl]piperazin-1-yl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CN(CC2)CCN2C2=NC(OCC(C=CC(C#N)=C3)=C3F)=CC=C2)=N2)=C2S1)=O YQEMYYJRRCXBIF-NRFANRHFSA-N 0.000 description 3
- HSOGTLPLNNSNLR-QFIPXVFZSA-N methyl 2-[[4-[6-[(4-cyano-2-fluorophenyl)methoxy]pyridin-2-yl]piperidin-1-yl]methyl]-3-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N=C(CN(CC2)CCC2C2=NC(OCC(C=CC(C#N)=C3)=C3F)=CC=C2)N2C[C@H]3OCC3)=C2S1)=O HSOGTLPLNNSNLR-QFIPXVFZSA-N 0.000 description 3
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- PJVMBPCXMUMTGK-QFIPXVFZSA-N methyl 2-[[4-[6-[(4-cyano-2-fluorophenyl)methoxy]pyridin-2-yl]-2-fluorophenyl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CC(C=CC(C2=NC(OCC(C=CC(C#N)=C3)=C3F)=CC=C2)=C2)=C2F)=N2)=C2S1)=O PJVMBPCXMUMTGK-QFIPXVFZSA-N 0.000 description 1
- YVSBSYNKORJRPP-QFIPXVFZSA-N methyl 2-[[4-[6-[(4-cyano-2-fluorophenyl)methoxy]pyridin-2-yl]-3,6-dihydro-2H-pyridin-1-yl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CN(CC2)CC=C2C2=NC(OCC(C=CC(C#N)=C3)=C3F)=CC=C2)=N2)=C2S1)=O YVSBSYNKORJRPP-QFIPXVFZSA-N 0.000 description 1
- WXOOFNSIHBLMJX-FQEVSTJZSA-N methyl 2-[[4-[6-[(4-cyano-2-fluorophenyl)methoxy]pyridin-2-yl]-6-oxopyridazin-1-yl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CN2N=CC(C3=NC(OCC(C=CC(C#N)=C4)=C4F)=CC=C3)=CC2=O)=N2)=C2S1)=O WXOOFNSIHBLMJX-FQEVSTJZSA-N 0.000 description 1
- OPPHJHRHHFTSBG-QHCPKHFHSA-N methyl 2-[[4-[6-[(4-cyano-2-fluorophenyl)methoxy]pyridin-2-yl]phenyl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CC(C=C2)=CC=C2C2=NC(OCC(C=CC(C#N)=C3)=C3F)=CC=C2)=N2)=C2S1)=O OPPHJHRHHFTSBG-QHCPKHFHSA-N 0.000 description 1
- PZKPYKMZTLPECE-QFIPXVFZSA-N methyl 2-[[4-[6-[(4-cyano-2-fluorophenyl)methoxy]pyridin-2-yl]piperidin-1-yl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CN(CC2)CCC2C2=NC(OCC(C=CC(C#N)=C3)=C3F)=CC=C2)=N2)=C2S1)=O PZKPYKMZTLPECE-QFIPXVFZSA-N 0.000 description 1
- KKLJOKWMBUQPOE-QFIPXVFZSA-N methyl 2-[[4-[6-[(4-cyanophenyl)methoxy]-5-fluoropyridin-2-yl]-2-fluorophenyl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CC(C=CC(C(C=C2)=NC(OCC(C=C3)=CC=C3C#N)=C2F)=C2)=C2F)=N2)=C2S1)=O KKLJOKWMBUQPOE-QFIPXVFZSA-N 0.000 description 1
- JPCNDFJIWJYERG-QHCPKHFHSA-N methyl 2-[[4-[6-[(4-cyanophenyl)methoxy]pyridin-2-yl]-2-fluorophenyl]methyl]-1-[[(2S)-oxetan-2-yl]methyl]thieno[2,3-d]imidazole-5-carboxylate Chemical compound COC(C1=CC(N(C[C@H]2OCC2)C(CC(C=CC(C2=NC(OCC(C=C3)=CC=C3C#N)=CC=C2)=C2)=C2F)=N2)=C2S1)=O JPCNDFJIWJYERG-QHCPKHFHSA-N 0.000 description 1
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- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000009707 neogenesis Effects 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 230000000802 nitrating effect Effects 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- DNUTZBZXLPWRJG-UHFFFAOYSA-M piperidine-1-carboxylate Chemical compound [O-]C(=O)N1CCCCC1 DNUTZBZXLPWRJG-UHFFFAOYSA-M 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 230000000291 postprandial effect Effects 0.000 description 1
- 238000011533 pre-incubation Methods 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- VVWRJUBEIPHGQF-UHFFFAOYSA-N propan-2-yl n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)N=NC(=O)OC(C)C VVWRJUBEIPHGQF-UHFFFAOYSA-N 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- VNAUDIIOSMNXBA-UHFFFAOYSA-N pyrazolo[4,3-c]pyrazole Chemical group N1=NC=C2N=NC=C21 VNAUDIIOSMNXBA-UHFFFAOYSA-N 0.000 description 1
- RQGPLDBZHMVWCH-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole Chemical group C1=NC2=CC=NC2=C1 RQGPLDBZHMVWCH-UHFFFAOYSA-N 0.000 description 1
- GZTPJDLYPMPRDF-UHFFFAOYSA-N pyrrolo[3,2-c]pyrazole Chemical group N1=NC2=CC=NC2=C1 GZTPJDLYPMPRDF-UHFFFAOYSA-N 0.000 description 1
- 125000006085 pyrrolopyridyl group Chemical group 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- WMURCVNNVHRGLI-UHFFFAOYSA-N tert-butyl 4-[2-(4-chloro-2-fluorophenyl)-2-methyl-1,3-benzodioxol-4-yl]piperidine-1-carboxylate Chemical compound ClC1=CC(=C(C=C1)C1(OC2=C(O1)C=CC=C2C1CCN(CC1)C(=O)OC(C)(C)C)C)F WMURCVNNVHRGLI-UHFFFAOYSA-N 0.000 description 1
- NLIPVNKRDRZMAQ-UHFFFAOYSA-N tert-butyl 4-[6-[(4-cyano-2-fluorophenyl)methoxy]pyridin-2-yl]-1,4-diazepane-1-carboxylate Chemical compound CC(C)(C)OC(N(CCC1)CCN1C1=NC(OCC(C=CC(C#N)=C2)=C2F)=CC=C1)=O NLIPVNKRDRZMAQ-UHFFFAOYSA-N 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- 150000001467 thiazolidinediones Chemical class 0.000 description 1
- 125000001984 thiazolidinyl group Chemical group 0.000 description 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 description 1
- 150000003573 thiols Chemical group 0.000 description 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical class [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- AHZJKOKFZJYCLG-UHFFFAOYSA-K trifluoromethanesulfonate;ytterbium(3+) Chemical compound [Yb+3].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F AHZJKOKFZJYCLG-UHFFFAOYSA-K 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000012224 working solution Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- 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
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Obesity (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Emergency Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Description
Claims (11)
- PCT国内申请,权利要求书已公开。
Applications Claiming Priority (9)
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CN2020115572973 | 2020-12-25 | ||
CN202011557297 | 2020-12-25 | ||
CN202110109531 | 2021-01-27 | ||
CN2021101095314 | 2021-01-27 | ||
CN2021104033659 | 2021-04-16 | ||
CN202110403365 | 2021-04-16 | ||
CN2021110001759 | 2021-09-02 | ||
CN202111000175 | 2021-09-02 | ||
PCT/CN2021/141243 WO2022135572A1 (zh) | 2020-12-25 | 2021-12-24 | 一种五并五元环衍生物及其在医药上的应用 |
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CN (1) | CN115667238B (zh) |
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CN116323599A (zh) | 2020-08-06 | 2023-06-23 | 加舒布鲁姆生物公司 | 杂环glp-1激动剂 |
EP4204415A1 (en) | 2020-08-28 | 2023-07-05 | Gasherbrum Bio, Inc. | Heterocyclic glp-1 agonists |
WO2023025201A1 (zh) * | 2021-08-24 | 2023-03-02 | 南京明德新药研发有限公司 | 咪唑并环类化合物及其应用 |
CN115850296A (zh) * | 2021-12-03 | 2023-03-28 | 杭州先为达生物科技有限公司 | 一种噻吩并咪唑类化合物的晶型及其制备方法 |
WO2023125896A1 (zh) * | 2021-12-31 | 2023-07-06 | 海思科医药集团股份有限公司 | 一种glp-1激动剂中间体及其制备方法及在医药中的用途 |
WO2023130878A1 (zh) * | 2022-01-10 | 2023-07-13 | 海思科医药集团股份有限公司 | 一种glp-1激动剂盐及其晶型及在医药上的应用 |
WO2023246833A1 (zh) * | 2022-06-23 | 2023-12-28 | 西藏海思科制药有限公司 | 一种五并五元环衍生物的药物组合物及其在医药上的应用 |
TW202408504A (zh) * | 2022-06-23 | 2024-03-01 | 大陸商西藏海思科製藥有限公司 | 噻吩[2,3-d]咪唑類化合物的鹽及其晶型和在醫藥上的用途 |
WO2024102625A1 (en) | 2022-11-11 | 2024-05-16 | Eli Lilly And Company | Glucagon-like peptide 1 receptor agonists |
WO2024107781A1 (en) | 2022-11-16 | 2024-05-23 | Eli Lilly And Company | Glucagon-like peptide 1 receptor agonists |
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WO2020207474A1 (en) * | 2019-04-12 | 2020-10-15 | Qilu Regor Therapeutics Inc. | Glp-1r agonists and uses thereof |
WO2021249492A1 (zh) * | 2020-06-10 | 2021-12-16 | 南京明德新药研发有限公司 | 甲基取代的苯并二噁唑类化合物及其应用 |
CN113831337A (zh) * | 2020-06-24 | 2021-12-24 | 广州市恒诺康医药科技有限公司 | Glp-1受体激动剂及其药物组合物和用途 |
CN115698022A (zh) * | 2020-06-04 | 2023-02-03 | 杭州先为达生物科技有限公司 | 五元杂芳并咪唑类化合物及其应用 |
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EP1594847A2 (en) * | 2003-02-12 | 2005-11-16 | Transtech Pharma, Inc. | Substituted azole derivatives as therapeutic agents |
PL3555064T3 (pl) * | 2016-12-16 | 2023-03-06 | Pfizer Inc. | Agoności receptora GLP-1 i ich zastosowania |
KR20210106447A (ko) * | 2018-11-22 | 2021-08-30 | 치루 레고르 테라퓨틱스 인코포레이티드 | Glp-1r 효능제 및 그의 용도 |
CN113801136B (zh) * | 2020-06-16 | 2023-04-07 | 江苏恒瑞医药股份有限公司 | 咪唑并杂芳基类衍生物、其制备方法及其在医药上的应用 |
CN115850296A (zh) * | 2021-12-03 | 2023-03-28 | 杭州先为达生物科技有限公司 | 一种噻吩并咪唑类化合物的晶型及其制备方法 |
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WO2020207474A1 (en) * | 2019-04-12 | 2020-10-15 | Qilu Regor Therapeutics Inc. | Glp-1r agonists and uses thereof |
CN115698022A (zh) * | 2020-06-04 | 2023-02-03 | 杭州先为达生物科技有限公司 | 五元杂芳并咪唑类化合物及其应用 |
WO2021249492A1 (zh) * | 2020-06-10 | 2021-12-16 | 南京明德新药研发有限公司 | 甲基取代的苯并二噁唑类化合物及其应用 |
CN115697338A (zh) * | 2020-06-10 | 2023-02-03 | 南京明德新药研发有限公司 | 甲基取代的苯并二噁唑类化合物及其应用 |
CN113831337A (zh) * | 2020-06-24 | 2021-12-24 | 广州市恒诺康医药科技有限公司 | Glp-1受体激动剂及其药物组合物和用途 |
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WO2022135572A1 (zh) | 2022-06-30 |
TW202233181A (zh) | 2022-09-01 |
ZA202306652B (en) | 2024-03-27 |
EP4269399A1 (en) | 2023-11-01 |
MX2023007569A (es) | 2023-09-21 |
KR20230124956A (ko) | 2023-08-28 |
JP2024500949A (ja) | 2024-01-10 |
US20240124470A1 (en) | 2024-04-18 |
EP4269399A4 (en) | 2024-06-05 |
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AU2021405918A1 (en) | 2023-07-20 |
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