反応 #502142

ord-1b8a027b0d874789871fa3094d6d385d

反応方程式

CSc1nc(Cc2ccccc2C)[nH]c(=O)c1C#N
2-(2-methylbenzyl)-4-(methylsulphanyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile
OCCC1CCNCC1
2-(4-piperidinyl)ethan-1-ol
Cc1ccccc1Cc1nc(N2CCC(CCO)CC2)c(C#N)c(=O)[nH]1
title compound
Cc1ccccc1Cc1nc(N2CCC(CCO)CC2)c(C#N)c(=O)[nH]1
4-[4-(2-Hydroxyethyl)-1-piperidinyl]-2-(2-methylbenzyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他the crude product is purified by preparative HPLC

実験手順

0.1 g (0.37 mmol) of 2-(2-methylbenzyl)-4-(methylsulphanyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile is heated with 0.14 g (1.1 mmol) of 2-(4-piperidinyl)ethan-1-ol in 3 ml of acetonitrile at 90° C. under argon for five days. After cooling to room temperature, the crude product is purified by preparative HPLC. 13 mg (10% of theory) of the title compound are obtained as a colourless solid.

出典

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