HRID1695923

反应详情

EQUATION

反应方程式

HRID 1695923 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
110 °C

PROCEDURE

实验过程

A mixture of (Z)-tert-butyl 4-(5-((3,3-dimethylbutylimino)methyl)thiazol-2-yl)piperidine-1-carboxylate (290 mg, 0.76 mmol, 1 eq) and (S)-2-mercaptosuccinic acid (138 mg, 0.92 mmol, 1.2 eq) in toluene (20 mL) was heated at 110° C. for 18 hr. The excess solvent was concentrated in vacuo and the solids were collected by filtration. The solids were washed with water, toluene and dried to give 2-((5S)-2-(2-(1-(tert-butoxycarbonyl)piperidin-4-yl)thiazol-5-yl)-3-(3,3-dimethylbutyl)-4-oxothiazolidin-5-yl)acetic acid (390 mg, 90% yield). (M+1) 512. 1H NMR (CDCl3) δ 7.15 (m, 1H), 5.68 (m, 1H), 4.58-4.11 (m, 3H), 3.62 (m, 1H), 3.39-3.09 (m, 2H), 2.93-2.74 (m, 3H), 2.09 (m, 2H), 1.71-1.64 (m, 2H), 1.47 (s, 9H), 1.44 (m, 1H), 0.85 (s, 9H) ppm.

WORKUP

后处理

  1. concentrationThe excess solvent was concentrated in vacuo
  2. filtrationthe solids were collected by filtration
  3. washThe solids were washed with water, toluene
  4. customdried