反応 #502138

ord-efd4b121fc5140f99f2a0f85a51910ef

反応方程式

CSc1nc(Cc2ccccc2)[nH]c(=O)c1C#N
2-benzyl-4-(methylsulphanyl)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile
C1CCNCC1
piperidine
N#Cc1c(N2CCCCC2)nc(Cc2ccccc2)[nH]c1=O
title compound
N#Cc1c(N2CCCCC2)nc(Cc2ccccc2)[nH]c1=O
2-Benzyl-6-oxo-4-(1-piperidinyl)-1,6-dihydropyrimidine-5-carbonitrile

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The resulting crude product is then purified by preparative HPLC

実験手順

43 mg (0.17 mmol) of 2-benzyl-4-(methylsulphanyl)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile are suspended in 0.3 ml of acetonitrile and stirred with 42.7 mg (0.50 mmol) of piperidine at 85° C. for 16 h. The resulting crude product is then purified by preparative HPLC. 11 mg (22% of theory) of the title compound are obtained.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08088769B2uspto-grants-2012_01