Reacción #502139

ord-97928c0c89dc4e5faa340de47c3efca6

Ecuación de reacción

CSc1nc(Cc2cccc(C)c2)[nH]c(=O)c1C#N
2-(3-methylbenzyl)-4-(methylsulphanyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile
OCCC1CCNCC1
2-(4-piperidinyl)ethan-1-ol
Cc1cccc(Cc2nc(N3CCC(CCO)CC3)c(C#N)c(=O)[nH]2)c1
title compound
Cc1cccc(Cc2nc(N3CCC(CCO)CC3)c(C#N)c(=O)[nH]2)c1
4-[4-(2-Hydroxyethyl)-1-piperidinyl]-2-(3-methylbenzyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe crude product is purified by preparative HPLC

Procedimiento

0.1 g (0.37 mmol) of 2-(3-methylbenzyl)-4-(methylsulphanyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile is heated with 0.142 g (1.16 mmol) of 2-(4-piperidinyl)ethan-1-ol in 3 ml of acetonitrile at 90° C. under argon for seven days. After cooling to room temperature, the crude product is purified by preparative HPLC. 0.047 g (36% of theory) of the title compound is obtained as a colourless solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08088769B2uspto-grants-2012_01