HRID977212

反应详情

EQUATION

反应方程式

HRID 977212 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

1.37 g of tert-butyl 1-{3-[4-(5-oxo-1,2,4-oxadiazolin-3-yl)phenyl]-2-oxo-5-oxazolidinylcarbonyl}piperidine-4-carboxylate are dissolved in 50 ml of methanol and hydrogenated over Raney nickel. The reaction mixture is, subsequently filtered and the filtrate is concentrated in vacuo. The product obtained is treated with 20 ml of ethyl acetate, with heating, and the product, after cooling, is filtered off with suction. Tert-butyl 1-[3-(4-amidinophenyl)-2-oxo-5-oxazolidinylcarbonyl}piperid-4-yl-carboxylate is obtained, m.p. 160°.

WORKUP

后处理

  1. filtrationsubsequently filtered
  2. concentrationthe filtrate is concentrated in vacuo
  3. customThe product obtained
  4. temperaturewith heating
  5. temperaturethe product, after cooling
  6. filtrationis filtered off with suction