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【结 构 式】

【分子编号】55213

【品名】tert-butyl (1R,2S)-2-methoxy-1-{(2R,3S)-1-(4-methoxybenzyl)-5-oxo-3-[(Z)-1-propenyl]pyrrolidinyl}-2-methylpentylcarbamate

【CA登记号】

【 分 子 式 】C27H42N2O5

【 分 子 量 】474.64096

【元素组成】C 68.32% H 8.92% N 5.9% O 16.85%

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:(LXXII)

Addition of the lithium anion of tert-butyl propiolate (LXIX) to nitrone (LXVIII) in the presence of BF3·Et2O gave adduct (LXX). Reduction of the hydroxylamine (LXX), with concomitant cyclization by treatment with Zn and HOAc, produced pyrrolidone (LXXI). The propenyl group of (LXXII) was introduced by conjugate addition of the corresponding organocuprate reagent to the unsaturated lactam (LXXI). Acidic Boc group cleavage in (LXXII), followed by acetylation of the resultant amine, afforded acetamide (LXXIII). Oxidative cleavage of the p-methoxybenzyl group of (LXXIII) using ammonium cerium nitrate gave pyrrolidone (LXXIV), which was further protected as the N-Boc derivative (LXXV). Introduction of the cyano group in (LXXV) as in the above methods led to the common precursor (XXXVII).

1 Hanessian, S.; et al.; Total synthesis of A-315675: A potent inhibitor of influenza neuraminidase. J Am Chem Soc 2002, 124, 17, 4716.
2 Inhibitors of neuraminidases. WO 0128996 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XXXVII) 55180 tert-butyl (2R,3S,5R)-2-[(1R,2S)-1-(acetylamino)-2-methoxy-2-methylpentyl]-5-cyano-3-[(Z)-1-propenyl]-1-pyrrolidinecarboxylate C22H37N3O4 详情 详情
(LXVIII) 55210 {(Z,2R,3S)-2-[(tert-butoxycarbonyl)amino]-3-methoxy-3-methylhexylidene}(4-methoxybenzyl)ammoniumolate C21H34N2O5 详情 详情
(LXIX) 28925 tert-butyl propiolate 13831-03-3 C7H10O2 详情 详情
(LXX) 55211 tert-butyl (5R,6S)-5-[(tert-butoxycarbonyl)amino]-4-[hydroxy(4-methoxybenzyl)amino]-6-methoxy-6-methyl-2-nonynoate C28H44N2O7 详情 详情
(LXXI) 55212 tert-butyl (1R,2S)-2-methoxy-1-[(2R)-1-(4-methoxybenzyl)-5-oxo-2,5-dihydro-1H-pyrrol-2-yl]-2-methylpentylcarbamate C24H36N2O5 详情 详情
(LXXII) 55213 tert-butyl (1R,2S)-2-methoxy-1-{(2R,3S)-1-(4-methoxybenzyl)-5-oxo-3-[(Z)-1-propenyl]pyrrolidinyl}-2-methylpentylcarbamate C27H42N2O5 详情 详情
(LXXIII) 55214 N-((1R,2S)-2-methoxy-1-{(2R,3S)-1-(4-methoxybenzyl)-5-oxo-3-[(Z)-1-propenyl]pyrrolidinyl}-2-methylpentyl)acetamide C24H36N2O4 详情 详情
(LXXIV) 55215 N-((1R,2S)-2-methoxy-2-methyl-1-{(2R,3S)-5-oxo-3-[(Z)-1-propenyl]pyrrolidinyl}pentyl)acetamide C16H28N2O3 详情 详情
(LXXV) 55216 tert-butyl (2R,3S)-2-[(1R,2S)-1-(acetylamino)-2-methoxy-2-methylpentyl]-5-oxo-3-[(Z)-1-propenyl]-1-pyrrolidinecarboxylate C21H36N2O5 详情 详情
Extended Information