• English
  • 简体中文
Login Register
Current Location: Home > Feedback Help Print

【结 构 式】

【分子编号】34305

【品名】ethyl (2S)-2-amino-4-(methylsulfanyl)butanoate

【CA登记号】

【 分 子 式 】C7H15NO2S

【 分 子 量 】177.26764

【元素组成】C 47.43% H 8.53% N 7.9% O 18.05% S 18.09%

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:(V)

The condensation of N-formyl-4-fluorophenylalanine (I) with 3-[bis(2-chloroethyl)amino]phenylalanine ethyl ester (II) by means of dicyclohexylcarbodiimide in THF gives N-formyl-4-fluoro-L-phenylalanyl-3-[bis(2-chloroethyl)amino]-L-phenylalanine ethyl ester (III), which is saponified with NaOH in DMF water yielding the free acid (IV). The condensation of (IV) with L-methionine ethyl ester (V) by means of N-hydroxysuccinimide and dicyclohexylcarbodiimide in DMF affords N-formyl-4-fluoro-L-phenylalanyl-3-[bis(2-chloroethyl)amino]phenylalanyl-L-methionine ethyl ester (VI), which is finally deprotected by elimination of the formyl group in ethanolic HCl.

1 De Barbieri, A.; et al.; Synthesis, acute toxicity and chemotherapeutic anti-cancer activities of a new tripeptidic mustard. Farm Sci Ed 1983, 38, 4, 205-218.
2 De Barbieri, A.; Compounds of dichlorodiethylaminophenylalanine with anti-tumor activity. EP 0056565; ES 8206449; IT 1134503; JP 57120559; US 4428875 .
3 Castaner, J.; Serradell, M.N.; PTT-119. Drugs Fut 1984, 9, 10, 753.
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) 34301 (2S)-3-(4-fluorophenyl)-2-(formylamino)propionic acid C10H10FNO3 详情 详情
(II) 34302 ethyl (2S)-2-amino-3-[3-[bis(2-chloroethyl)amino]phenyl]propanoate C15H22Cl2N2O2 详情 详情
(III) 34303 ethyl (2S)-3-[3-[bis(2-chloroethyl)amino]phenyl]-2-[[(2S)-3-(4-fluorophenyl)-2-(formylamino)propanoyl]amino]propanoate C25H30Cl2FN3O4 详情 详情
(IV) 34304 (2S)-3-[3-[bis(2-chloroethyl)amino]phenyl]-2-[[(2S)-3-(4-fluorophenyl)-2-(formylamino)propanoyl]amino]propionic acid C23H26Cl2FN3O4 详情 详情
(V) 34305 ethyl (2S)-2-amino-4-(methylsulfanyl)butanoate C7H15NO2S 详情 详情
(VI) 34306 ethyl (2S)-2-[((2S)-3-[3-[bis(2-chloroethyl)amino]phenyl]-2-[[(2S)-3-(4-fluorophenyl)-2-(formylamino)propanoyl]amino]propanoyl)amino]-4-(methylsulfanyl)butanoate C30H39Cl2FN4O5S 详情 详情
Extended Information