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【结 构 式】

【分子编号】40515

【品名】3-(dimethylamino)-1-(2-thienyl)-1-propanol

【CA登记号】

【 分 子 式 】C9H15NOS

【 分 子 量 】185.29024

【元素组成】C 58.34% H 8.16% N 7.56% O 8.63% S 17.31%

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:(VII)

The ketone intermediate (II) can also be reduced with NaBH4 in ethanol to the racemic alcohol (VII), which is submitted to optical resolution with (S)-(+)-mandelic acid to provide the (S)-enantiomer (IV) already described.

1 Sorbera, L.A.; Castaner, R.M.; Castaner, J.; Duloxetine oxalate. Drugs Fut 2000, 25, 9, 907.
2 Berglund, R.A. (Eli Lilly and Company); Asymmetric synthesis. EP 0650965; JP 1995188065; US 5362886 .
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) 24490 1-(2-Thienyl)-1-ethanone; 2-Acetylthiophene 88-15-3 C6H6OS 详情 详情
(II) 40500 3-(dimethylamino)-1-(2-thienyl)-1-propanone 13196-35-5 C9H13NOS 详情 详情
(IV) 40502 (1S)-3-(dimethylamino)-1-(2-thienyl)-1-propanol 116817-84-6 C9H15NOS 详情 详情
(VII) 40515 3-(dimethylamino)-1-(2-thienyl)-1-propanol C9H15NOS 详情 详情
Extended Information