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【结 构 式】

【分子编号】42153

【品名】methyl (2S,3R,4S,5R,6S)-3,4,5-tris(acetoxy)-6-[4-[(2S,3R)-3-[(3S)-3-(acetoxy)-3-(4-fluorophenyl)propyl]-1-(4-fluorophenyl)-4-oxoazetidinyl]phenoxy]tetrahydro-2H-pyran-2-carboxylate

【CA登记号】

【 分 子 式 】C39H39F2NO13

【 分 子 量 】767.7344064

【元素组成】C 61.01% H 5.12% F 4.95% N 1.82% O 27.09%

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:(VI)

Diol (III) was acetylated with Ac2O in the presence of dimethylaminopyridine to yield diester (IV), which was selectively hydrolyzed to monoacetate (V) by means of methanolic guanidine. Coupling of phenol (V) with imidate (II) by means of boron trifluoride etherate furnished the protected glucuronide (VI). The ester groups of (VI) were finally hydrolyzed by treatment with triethylamine in aqueous methanol.

1 Yumibe, N.P.; Alton, K.B.; Van Heek, M.; Davis, H.R.; Vaccaro, W.D. (Schering Corp.); Sugar-substd. 2-azetidinones useful as hypocholesterolemic agents. EP 0877750; JP 1998512592; WO 9716455 .
2 Yumibe, N.P.; Alton, K.B.; Vaccaro, W.D.; Davis, H.R.; Van Heek, M. (Schering Corp.); Sugar-substd. 2-azetidinones useful as hypocholesterolemic agents. US 5756470 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(II) 42149 methyl (2S,3R,4S,5R,6S)-3,4,5-tris(acetoxy)-6-[(2,2,2-trichloroethanimidoyl)oxy]tetrahydro-2H-pyran-2-carboxylate C15H18Cl3NO10 详情 详情
(III) 42150 (3R,4S)-1-(4-fluorophenyl)-3-[(3S)-3-(4-fluorophenyl)-3-hydroxypropyl]-4-(4-hydroxyphenyl)-2-azetidinone C24H21F2NO3 详情 详情
(IV) 42151 4-[(2S,3R)-3-[(3S)-3-(acetoxy)-3-(4-fluorophenyl)propyl]-1-(4-fluorophenyl)-4-oxoazetidinyl]phenyl acetate C28H25F2NO5 详情 详情
(V) 42152 (1S)-1-(4-fluorophenyl)-3-[(2S,3R)-1-(4-fluorophenyl)-2-(4-hydroxyphenyl)-4-oxoazetidinyl]propyl acetate C26H23F2NO4 详情 详情
(VI) 42153 methyl (2S,3R,4S,5R,6S)-3,4,5-tris(acetoxy)-6-[4-[(2S,3R)-3-[(3S)-3-(acetoxy)-3-(4-fluorophenyl)propyl]-1-(4-fluorophenyl)-4-oxoazetidinyl]phenoxy]tetrahydro-2H-pyran-2-carboxylate C39H39F2NO13 详情 详情
Extended Information