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【结 构 式】

【分子编号】42334

【品名】ethyl (2R)-2-amino-2-phenylethanoate

【CA登记号】17609-48-2

【 分 子 式 】C10H13NO2

【 分 子 量 】179.21876

【元素组成】C 67.02% H 7.31% N 7.82% O 17.85%

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:(II)

D-Phenylglycine (I) was converted to ethyl ester (II) by means of ethanol and thionyl chloride. Coupling of N-Fmoc-S-benzylcysteine (III) with amino ester (II) produced the protected dipeptide (IV). The Fmoc group of (IV) was then removed by treatment with piperidine in DMF to give (V). N-Fmoc-glutamic acid alpha-benzyl ester (VII) was prepared by reaction of glutamic acid alpha-benzyl ester (VI) with N-(fluorenylmethoxycarbonyloxy)succinimide. Coupling of protected glutamic acid (VII) with dipeptide (V) furnished tripeptide (VIII). The Fmoc and ester protecting groups of (VIII) were finally cleaved by treatment with NaOH.

1 Lyttle, M.H.; et al.; Isozyme-specific glutathione-S-transferase: Design and synthesis. J Med Chem 1994, 37, 1, 189.
2 Kauvar, L.M.; Lyttle, M.H. (Telik, Inc.); Glutathione analogs and paralog panels comprising glutathione mimics. EP 0720620; US 5599903; WO 9508563 .
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) 40170 (2R)-2-amino-2-phenylethanoic acid C8H9NO2 详情 详情
(II) 42334 ethyl (2R)-2-amino-2-phenylethanoate 17609-48-2 C10H13NO2 详情 详情
(III) 42335 (2R)-3-(benzylsulfanyl)-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]propionic acid C25H23NO4S 详情 详情
(IV) 42336 ethyl (2R)-2-[((2R)-3-(benzylsulfanyl)-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]propanoyl)amino]-2-phenylethanoate C35H34N2O5S 详情 详情
(V) 42337 ethyl (2R)-2-[[(2R)-2-amino-3-(benzylsulfanyl)propanoyl]amino]-2-phenylethanoate C20H24N2O3S 详情 详情
(VI) 42338 (4S)-4-amino-5-(benzyloxy)-5-oxopentanoic acid 13030-09-6 C12H15NO4 详情 详情
(VII) 42339 (4S)-5-(benzyloxy)-4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-5-oxopentanoic acid C27H25NO6 详情 详情
(VIII) 42340 5-benzyl 13-ethyl (5S,10R,13R)-10-[(benzylsulfanyl)methyl]-1-(9H-fluoren-9-yl)-3,8,11-trioxo-13-phenyl-2-oxa-4,9,12-triazatridecane-5,13-dicarboxylate C47H47N3O8S 详情 详情
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