Реакция #1577

ord-9562367f4fb64f8a9fa6a9e9643f95bb

Уравнение реакции

C#CCNC(=O)Nc1cc(NC(C)=O)c(F)cc1Cl
1-(5-acetamido-2-chloro-4-fluorophenyl)-3-(2-propynyl)urea
c1ccncc1
pyridine
c1ccncc1
pyridine
O=C=NC(=O)Cl
N-(chlorocarbonyl) isocyanate
O=C=NC(=O)Cl
N-(chlorocarbonyl) isocyanate
C#CCn1c(=O)[nH]c(=O)n(-c2cc(NC(C)=O)c(F)cc2Cl)c1=O
title product
C#CCn1c(=O)[nH]c(=O)n(-c2cc(NC(C)=O)c(F)cc2Cl)c1=O
4'-Chloro-2'-fluoro-5'-[hexahydro-2,4,6-trioxo-3-(2-propynyl)-s-triazin-1-yl]acetanilide

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураrefluxed for 90 minutes
  2. 2
    Температураcooled to room temperature
  3. 3
    workup.STIRRINGstirred for 10 minutes
  4. 4
    Температураcooled to room temperature
  5. 5
    Фильтрацияfiltered
  6. 6
    Другоеto obtain a solid
  7. 7
    ПромывкаThe solid is washed sequentially with water and hexanes
  8. 8
    Другоеdried

Методика

A mixture of 1-(5-acetamido-2-chloro-4-fluorophenyl)-3-(2-propynyl)urea (4.50 g, 15.9 mmol), and pyridine (2.56 mL, 31.8 mmol) in methylene chloride is treated with N-(chlorocarbonyl) isocyanate (1.92 mL, 23.9 mmol), stirred at room temperature overnight, refluxed for 90 minutes, cooled to room temperature, treated with additional pyridine (1.30 mL) and N-(chlorocarbonyl) isocyanate (1.92 mL), stirred for 10 minutes, cooled to room temperature, and filtered to obtain a solid. The solid is washed sequentially with water and hexanes, and dried to give the title product as a tan solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726126uspto-grants-1998_03