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【结 构 式】

【分子编号】66890

【品名】2-(3-((tert-butyldimethylsilyl)oxy)benzyl)-1-((N-methylphenylsulfonimidoyl)methyl)-4-((tetrahydro-2H-pyran-2-yl)peroxy)-3-(3-((tetrahydro-2H-pyran-2-yl)peroxy)octyl)cyclopentanol

【CA登记号】 

【 分 子 式 】C44H71NO9SSi

【 分 子 量 】818.201

【元素组成】C 64.59% H 8.75% N 1.71% O 17.60% S 3.92% Si 3.42%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(VII)

 

1 Aristoff PA. 1987. Interphenylene carbacyclin derivatives. US 4683330(本专利属于The Upjohn Compa- ny) Aristoff PA 1981.Composition and pro卧US 4306075(本专利■于The Upjohn Company) Aristoff PA. 1982,Methno carbacyclin analogs US 4349689(本专利属于The Upjohn Company)
2 Aristoff PA. 1981.Composition and process. US 4306075(本专利属于The Upjohn Company)
3 Aristoff PA. 1982. Methno carbacyclin analogs. US 4349689(本专利属于The Upjohn Company)
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 14647 5-methoxy-3,4-dihydro-2(1H)-naphthalenone 32940-15-1 C11H12O2 详情 详情
(II) 46567 (3aS)-5-methoxy-3a,4-dihydronaphtho[2,3-b]furan-2(3H)-one C13H12O3 详情 详情
(III) 46566 dimethyl (4S)-4-(tetrahydro-2H-pyran-2-yloxy)nonylphosphonate C16H33O5P 详情 详情
(IV) 46568 (9aS)-8-methoxy-3-[(3S)-3-(tetrahydro-2H-pyran-2-yloxy)octyl]-1,4,9,9a-tetrahydro-2H-cyclopenta[b]naphthalen-2-one C27H38O4 详情 详情
(VI) 46549 (2R,3R,4R)-2-(3-[[tert-butyl(dimethyl)silyl]oxy]benzyl)-4-(tetrahydro-2H-pyran-2-yloxy)-3-[(E,3S)-3-(tetrahydro-2H-pyran-2-yloxy)-1-octenyl]cyclopentanone C36H58O6Si 详情 详情
(VII) 66890 2-(3-((tert-butyldimethylsilyl)oxy)benzyl)-1-((N-methylphenylsulfonimidoyl)methyl)-4-((tetrahydro-2H-pyran-2-yl)peroxy)-3-(3-((tetrahydro-2H-pyran-2-yl)peroxy)octyl)cyclopentanol   C44H71NO9SSi 详情 详情
(VIII) 46555 [(1S,2S,3S,4R)-2-(3-hydroxybenzyl)-4-(tetrahydro-2H-pyran-2-yloxy)-3-[(E,3S)-3-(tetrahydro-2H-pyran-2-yloxy)-1-octenyl]cyclopentyl]methyl methanesulfonate C32H50O8S 详情 详情
(IX) 46556 (1S,2R,3aS,9aS)-2-(tetrahydro-2H-pyran-2-yloxy)-1-[(E,3S)-3-(tetrahydro-2H-pyran-2-yloxy)-1-octenyl]-2,3,3a,4,9,9a-hexahydro-1H-cyclopenta[b]naphthalen-5-ol C31H46O5 详情 详情
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