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Resolution of 3-(methylamino)-1-(2-thienyl)propan-1-ol, a new key intermediate for duloxetine, with (S)-mandelic acid

机译:用(S)-扁桃酸拆分3-(甲基氨基)-1-(2-噻吩基)丙-1-醇(度洛西汀的新关键中间体)

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摘要

The resolution of racemic 3-(methylamino)-1-(2-thienyl)propan-1-ol (3), a new key intermediate for duloxetine (1), was studied. The conditions were optimized for an industrial-scale resolution of 3 by using (S)-mandelic acid (4) as a resolving agent and 2-butanol containing two equimolar amounts of water as a solvent. The (S)-3・(S)-4・H2O diastereomeric salt was crystallized to give pure (S)-3 with >99.9% ee after liberation of the amine. Absolute configuration of liberated (-)-3 was determined as (S)-form by X-ray crystallography.
机译:研究了消旋3-(甲基氨基)-1-(2-噻吩基)丙-1-醇(3)(度洛西汀(1)的新关键中间体)的拆分。通过使用(S)-扁桃酸(4)作为拆分剂和含有两个等摩尔量的水作为溶剂的2-丁醇,将条件优化为3的工业规模分辨率。胺释放后,将(S)-3 ・(S)-4 ・ H2O非对映异构体盐结晶,得到纯净的(S)-3,其ee> 99.9%。通过X射线晶体学测定释放的(-)-3的绝对构型为(S)形式。

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