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【结 构 式】

【分子编号】25326

【品名】benzyl (2S)-2-[[chloro(phenoxy)phosphoryl]amino]propanoate

【CA登记号】

【 分 子 式 】C16H17ClNO4P

【 分 子 量 】353.741782

【元素组成】C 54.33% H 4.84% Cl 10.02% N 3.96% O 18.09% P 8.76%

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)

Title phosphoramidate was obtained by condensation of phenyl [(1-naphthylmethoxy)alanino]phosphorochloridate (I) with 2',3'-dideoxy-2',3'-didehydrothymidine (II) in the presence of N-methylmorpholine in THF at r.t.

1 McGuigan, C.; Sutton, P.W.; Cahard, D.; Turner, K.; O'Leary, G.; Wang, Y.; Gumbleton, M.; De Clercq, E.; Balzarini, J.; Synthesis, anti-human immunodeficiency virus activity and esterase lability of some novel carboxylic ester-modified phosphoramidate derivatives of stavudine (d4T). Antivir Chem Chemother 1998, 9, 6, 473.
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) 25326 benzyl (2S)-2-[[chloro(phenoxy)phosphoryl]amino]propanoate C16H17ClNO4P 详情 详情
(II) 25323 1-[(2R,5S)-5-(hydroxymethyl)-2,5-dihydro-2-furanyl]-5-methyl-2,4(1H,3H)-pyrimidinedione C10H12N2O4 详情 详情
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