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【结 构 式】

【分子编号】31814

【品名】benzyl (3R)-3-hydroxy-13-methyltetradecanoate

【CA登记号】

【 分 子 式 】C22H36O3

【 分 子 量 】348.52604

【元素组成】C 75.82% H 10.41% O 13.77%

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:(I)

Condensation of (R)-benzyl 3-hydroxy-13-methyl tetradecanoate (I) with N-Boc-L-isoleucine (II) in the presence of dicyclohexyl carbodiimide and dimethylaminopyridine furnished the corresponding ester (III). After deprotection of the benzyl group of (III) by hydrogenation over Pd/C, the resulting carboxylic acid (IV) was attached to an oxime resin using O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU) to give the resin-coupled product (V).

1 Yanai, M.; Suguroi, T.; Solid-phase synthesis of cyclooctadepsipeptide N-4909 using a cyclization-cleavage method with oxime resin. J Antibiot 1999, 52, 9, 835.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IV),(V) 31816 (3S)-3-([(2S,3S)-2-[(tert-butoxycarbonyl)amino]-3-methylpentanoyl]oxy)-13-methyltetradecanoic acid C26H49NO6 详情 详情
(I) 31814 benzyl (3R)-3-hydroxy-13-methyltetradecanoate C22H36O3 详情 详情
(II) 30009 (2S,3S)-2-[(tert-butoxycarbonyl)amino]-3-methylpentanoic acid 13139-16-7 C11H21NO4 详情 详情
(III) 31815 benzyl (3S)-3-([(2S,3S)-2-[(tert-butoxycarbonyl)amino]-3-methylpentanoyl]oxy)-13-methyltetradecanoate C33H55NO6 详情 详情
Extended Information