Реакция #502137

ord-17816114ba774dbab023c742b6a0f60a

Уравнение реакции

CSc1nc(Cc2ccc(Cl)c(Cl)c2)[nH]c(=O)c1C#N
2-(3,4-dichlorobenzyl)-4-(methylsulphanyl)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile
C1CCNCC1
piperidine
N#Cc1c(N2CCCCC2)nc(Cc2ccc(Cl)c(Cl)c2)[nH]c1=O
title compound
N#Cc1c(N2CCCCC2)nc(Cc2ccc(Cl)c(Cl)c2)[nH]c1=O
2-(3,4-Dichlorobenzyl)-6-oxo-4-(1-piperidinyl)-1,6-dihydropyrimidine-5-carbonitrile

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеAfter removal of the volatile constituents in vacuo
  2. 2
    Другоеthe residue is purified by preparative HPLC

Методика

100 mg (0.34 mmol) of 2-(3,4-dichlorobenzyl)-4-(methylsulphanyl)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile are stirred with 261 mg (3.07 mmol) of piperidine at 85° C. for 16 h. After removal of the volatile constituents in vacuo, the residue is purified by preparative HPLC. 42 mg (38% of theory) of the title compound are obtained.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08088769B2uspto-grants-2012_01