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【结 构 式】

【分子编号】31190

【品名】2-[(2-thienylcarbonyl)sulfanyl]propionic acid

【CA登记号】

【 分 子 式 】C8H8O3S2

【 分 子 量 】216.28172

【元素组成】C 44.43% H 3.73% O 22.19% S 29.65%

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:(III)

Triethylamine is added to thiolactic acid (I) and 2-thiophencarbonyl chloride (II) in tetrahydrofuran. Mix is cooled at -5 C under agitation and thionyl chloride is added keeping the temperature between 0 and 10 C. A solution of homocysteine thiolactone hydrochloride and triethylamine in water is then added to the reaction, keeping the temperature below 10 C. The reaction is carried out for 1 h at room temperature under agitation, after which the solvent is evaporated at reduced pressure. Water is used to wash and diethyl ether to extract. The organic phase is dried on Na2SO4 anhydrous and the solvent is eliminated at reduced pressure. The raw product obtained from a mix of dichloromethane/diethyl ether (60/40) is crystallized (MR-889).

1 Quadro, G.; MR-889. Drugs Fut 1990, 15, 10, 997.
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) 24361 2-sulfanylpropionic acid; 2-mercaptopropionic acid 57965-30-7 C3H6O2S 详情 详情
(II) 14103 2-Thiophenecarbonyl chloride 5271-67-0 C5H3ClOS 详情 详情
(III) 31190 2-[(2-thienylcarbonyl)sulfanyl]propionic acid C8H8O3S2 详情 详情
(IV) 31191 S-(2-chloro-1-methyl-2-oxoethyl) 2-thiophenecarbothioate C8H7ClO2S2 详情 详情
(V) 22495 3-aminodihydro-2(3H)-thiophenone 10593-85-8 C4H7NOS 详情 详情
Extended Information