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【结 构 式】

【分子编号】63823

【品名】methyl (5S,7R)-5-ethyl-7-({[(4-methylphenyl)sulfonyl]oxy}methyl)-3-[(4-nitrophenyl)sulfonyl]-5-[(2,2,2-trifluoroacetyl)oxy]-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino[5,4-b]indole-9-carboxylate

【CA登记号】

【 分 子 式 】C36H38F3N3O11S2

【 分 子 量 】809.8385496

【元素组成】C 53.39% H 4.73% F 7.04% N 5.19% O 21.73% S 7.92%

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:(XLIX)

Acid-catalyzed deprotection of the N-Boc and O-silyl groups of (XLV) leads to (XLVI). The primary hydroxyl group of (XLVI) is then tosylated to afford (XLVII). Subsequent esterification of the remaining tertiary hydroxyl with trifluoroacetic anhydride and pyridine yields trifluoroacetate (XLVIII). Chlorination of the indole nucleus of (XLVIII) with t-butyl hypochlorite furnishes the chloroindolenine (XLIX). Thisi is then coupled to vindoline (XXIII) in the presence of trifluoroacetic acid to form the bis-indole adduct (L) (8,9).

1 Yokoshima, S.; Ueda, T.; Kobayashi, S.; Sato, A.; Kuboyama, T.; Tokuyama, H.; Fukuyama, T.; Stereocontrolled total synthesis of (+)-vinblastine. J Am Chem Soc 2002, 124, 10, 2137.
2 Schneider, C.; First de novo synthesis of the bisindole alkaloid vinblastine. Angew Chem. Int Ed 2002, 41, 22, 4217.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XXIV) 63596 methyl 4-(acetyloxy)-3a-ethyl-5-hydroxy-6-methyl-8-(methyloxy)-3a,4,5,5a,6,11,12,13a-octahydro-1H-indolizino[8,1-cd]carbazole-5-carboxylate C25H32N2O6 详情 详情
(XLVI) 63816 10-(tert-butyl) 9-methyl (5S,7R)-7-({[tert-butyl(diphenyl)silyl]oxy}methyl)-5-ethyl-5-hydroxy-3-[(4-nitrophenyl)sulfonyl]-2,3,4,5,6,7,8,9-octahydroazacycloundecino[5,4-b]indole-9,10(1H)-dicarboxylate C48H59N3O10SSi 详情 详情
(XLVII) 63821 methyl (5S,7R)-5-ethyl-5-hydroxy-7-(hydroxymethyl)-3-[(4-nitrophenyl)sulfonyl]-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino[5,4-b]indole-9-carboxylate C27H33N3O8S 详情 详情
(XLVIII) 63822 methyl (5S,7R)-5-ethyl-5-hydroxy-7-({[(4-methylphenyl)sulfonyl]oxy}methyl)-3-[(4-nitrophenyl)sulfonyl]-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino[5,4-b]indole-9-carboxylate C34H39N3O10S2 详情 详情
(XLIX) 63823 methyl (5S,7R)-5-ethyl-7-({[(4-methylphenyl)sulfonyl]oxy}methyl)-3-[(4-nitrophenyl)sulfonyl]-5-[(2,2,2-trifluoroacetyl)oxy]-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino[5,4-b]indole-9-carboxylate C36H38F3N3O11S2 详情 详情
(L) 63824 methyl (5S,7R)-14b-chloro-5-ethyl-7-({[(4-methylphenyl)sulfonyl]oxy}methyl)-3-[(4-nitrophenyl)sulfonyl]-5-[(2,2,2-trifluoroacetyl)oxy]-1,2,3,4,5,6,7,8,10,14b-decahydroazacycloundecino[5,4-b]indole-9-carboxylate C36H37ClF3N3O11S2 详情 详情
(LI) 63825 methyl (3aR,4R,5S,5aR,10bR,13aR)-4-(acetyloxy)-3a-ethyl-9-{(5S,7R,9S)-5-ethyl-9-(methoxycarbonyl)-7-({[(4-methylphenyl)sulfonyl]oxy}methyl)-3-[(4-nitrophenyl)sulfonyl]-5-[(2,2,2-trifluoroacetyl)oxy]-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino[5,4 C61H68F3N5O17S2 详情 详情
Extended Information