HRID1297243

反应详情

EQUATION

反应方程式

HRID 1297243 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a solution of (1-carbamoyl-2-isobutyl-cyclopropylmethyl)-carbamic acid tert-butyl ester (5.8 g, 21.5 mmol) in dry DMF (100 mL) was added cyanuric chloride (5.5 g, 30.1 mmol). The reaction mixture was stirred at 0° C. for 30 minutes and was poured into cold 0.5N NaOH (200 mL). The aqueous phase was extracted with EtOAc (2×150 mL) and the combined organic layer was washed with water and brine and dried over Na2SO4. Removal of excess of solvent, followed by purification of the residue by flash column chromatography using hexanes/EtOAc (9:1) as eluent gave 4.9 g (91%) of (1-cyano-2-isobutyl-cyclopropylmethyl)-carbamic acid tert-butyl ester as a colorless foam: 1H NMR (300 MHz, CDCl3) δ 0.86 (m, 1H), 0.94 (d, J=4.0 Hz, 3H), 0.96 (d, J=4.0 Hz, 3H), 1.56 (m, 1H), 1.37-1.56 (m, 12H), 1.71 (m, 1H), 3.32 (d, J=6.1 Hz, 2H), 5.26 (s, 1H); 13C (75 MHz, CDCl3) δ 14.5, 18.8, 21.9, 22.2, 24.4, 28.0, 28.1, 36.3, 40.4, 79.3, 122.9, 155.4; MS (APCI) m/z 253 [M+H]+.

WORKUP

后处理

  1. extractionThe aqueous phase was extracted with EtOAc (2×150 mL)
  2. washthe combined organic layer was washed with water and brine
  3. dry with materialdried over Na2SO4
  4. customRemoval of excess of solvent
  5. customfollowed by purification of the residue by flash column chromatography