반응 #502141

ord-a74ca523dc074f7089324fcd3641a6a2

반응 방정식

CSc1nc(Cc2cccc(C)c2)[nH]c(=O)c1C#N
2-(3-methylbenzyl)-4-(methylsulphanyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile
OC[C@@H]1CCCN1
(S)-(+)-2-pyrrolidinemethanol
Cc1cccc(Cc2nc(N3CCC[C@H]3CO)c(C#N)c(=O)[nH]2)c1
title compound
Cc1cccc(Cc2nc(N3CCC[C@H]3CO)c(C#N)c(=O)[nH]2)c1
4-[(2S)-2-(Hydroxymethyl)-1-pyrrolidinyl]-2-(3-methylbenzyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the crude product is purified by preparative HPLC

실험 절차

0.1 g (0.37 mmol) of 2-(3-methylbenzyl)-4-(methylsulphanyl)-6-oxo-1,6-dihydro-5-pyrimidinecarbonitrile is heated with 0.11 g (1.1 mmol) of (S)-(+)-2-pyrrolidinemethanol 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. 0.035 g (29% of theory) of the title compound is obtained as a colourless solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08088769B2uspto-grants-2012_01