HRID47712

反应详情

EQUATION

反应方程式

HRID 47712 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

A mixture of 0.94 g of N-(tert-butyl)-N′-[(1R)-2-hydroxy-1-(3-thienylmethyl)ethyl]thiourea in 9.2 cm3 of 6N hydrochloric acid is heated at a temperature in the region of 100° C. with stirring for 3 hours and is then concentrated under reduced pressure (2 kPa) at a temperature in the region of 40° C. A greenish oil is obtained, which is taken up in 10 cm3 of acetone to give a sticky gum. 1.5 cm3 of ethanol are then added, followed by dropwise addition, with stirring, of 6 cm3 of diethyl ether. The crystals obtained are filtered off on a sinter funnel, washed with diethyl ether and then dried in an oven under vacuum (10 Pa) at a temperature in the region of 50° C. 0.5 g of (−)-(4R)-4-(3-thienylmethyl)-4,5-dihydro-1,3-thiazol-2-ylamine hydrochloride is obtained in the form of gray crystals melting at 152° C. 1H NMR spectrum (400 MHz, (CD3)2SO-d6, δ in ppm): 2.99 (mt: 2H); 3.26 (dd, J=11 and 5.5 Hz: 1H); 3.59 (dd, J=11 and 8 Hz: 1H); 4.54 (mt: 1H); 7.10 (dd, J=5.5 and 1 Hz: 1H); 7.38 (mt: 1H); 7.54 (dd, J=5 and 3 Hz: 1H); from 9.15 to 10.55 (broad unres. mult.: 3H). (αD20=−4.3±0.5 at a concentration of 0.5% in methanol).

WORKUP

后处理

  1. concentrationis then concentrated under reduced pressure (2 kPa) at a temperature in the region of 40° C
  2. customA greenish oil is obtained
  3. customto give a sticky gum
  4. additionfollowed by dropwise addition
  5. customThe crystals obtained
  6. filtrationare filtered off on a sinter funnel
  7. washwashed with diethyl ether
  8. customdried in an oven under vacuum (10 Pa) at a temperature in the region of 50° C