反应 #2314325

ord-b592233971e2435895af11c965a74d6e

反应方程式

COC1=NC(Cl)=NC(N)N1C(F)F
2-amino-4-chlorodifluoromethyl-6-methoxy-1,3,5-triazine
O=C=NS(=O)(=O)c1ccccc1[N+](=O)[O-]
2-nitrobenzenesulfonyl isocyanate
COC1=NC(Cl)=NC(NC(=O)NS(=O)(=O)c2ccccc2[N+](=O)[O-])N1C(F)F
title compound
收率 35.2%
COC1=NC(Cl)=NC(NC(=O)NS(=O)(=O)c2ccccc2[N+](=O)[O-])N1C(F)F
N-[(4-Chlorodifluoromethyl-6-methoxy-1,3,5-triazin-2-yl) aminocarbonyl]-2-nitrobenzenesulfonamide
收率 35.2%

反应条件

温度
25°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤the deposited product was filtered off with suction
  2. 2
    洗涤washed with a little ether
  3. 3
    干燥dried at 40° C. in a water-jet vacuum

实验过程

A solution of 4.2 g of 2-amino-4-chlorodifluoromethyl-6-methoxy-1,3,5-triazine (20 mmol) in 20 ml of methylene chloride was treated at 25° C. with a solution of 4.6 g of 2-nitrobenzenesulfonyl isocyanate (20 mmol) in 5 ml of methylene chloride. The mixture was subsequently stirred at 25° C. for 16 h, and the deposited product was filtered off with suction, washed with a little ether and dried at 40° C. in a water-jet vacuum. 3.1 g of the title compound (35% of theory) of m.p. 181° C. were thus obtained.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06413911B1uspto-grants-2002_07