Réaction #502140

ord-752e4d4ab0924b6bba17a49593e37006

Équation de réaction

CSc1nc(Cc2cccc(C)c2)[nH]c(=O)c1C#N
2-(3-methylbenzyl)-4-(methylsulphanyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile
NC1CCCC1
cyclopentylamine
Cc1cccc(Cc2nc(NC3CCCC3)c(C#N)c(=O)[nH]2)c1
title compound
Cc1cccc(Cc2nc(NC3CCCC3)c(C#N)c(=O)[nH]2)c1
4-(Cyclopentylamino)-2-(3-methylbenzyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe crude product is purified by preparative HPLC

Mode opératoire

0.1 g (0.37 mmol) of 2-(3-methylbenzyl)-4-(methylsulphanyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile is heated with 0.31 g (3.65 mmol) of cyclopentylamine in 3 ml of acetonitrile at 90° C. under argon overnight. After cooling to room temperature, the crude product is purified by preparative HPLC. 0.03 g (26% of theory) of the title compound is obtained as a colourless solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08088769B2uspto-grants-2012_01