Reacción #1755464

ord-4a3f3eb29cb9434ab7a79c73b63f651a

Ecuación de reacción

Cc1cc(C)cc(CC(NC(=S)NCCO)c2ccco2)c1
1-[2-(3,5-dimethylphenyl)-1-furan-2-yl-ethyl]-3-(2-hydroxy-ethyl)-thiourea
CCN(C(C)C)C(C)C
diisopropyethylamine
C[P+](C)(C)CC#N.[I-]
cyanomethyl trimethylphosphonium iodide
Cc1cc(C)cc(CC(NC2=NCCS2)c2ccco2)c1
title compound
Rendimiento 69.1%
Cc1cc(C)cc(CC(NC2=NCCS2)c2ccco2)c1
(4,5-Dihydro-thiazol-2-yl)-[2-(3,5-dimethyl-phenyl)-1-furan-2-yl-ethyl]-amine
Rendimiento 69.1%

Disolventes

Condiciones de reacción

Temperatura
90°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

Following the procedure as described in example a solution of 1-[2-(3,5-dimethylphenyl)-1-furan-2-yl-ethyl]-3-(2-hydroxy-ethyl)-thiourea (0.46 g) and diisopropyethylamine (0.26 g) in propionitrile (20 ml) was treated with cyanomethyl trimethylphosphonium iodide (0.44 g) and heated for 16 h at a temperature of 90° C. Work-up yielded the title compound (0.30 g, 69%) as an amorphous solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07989394B2uspto-grants-2011_08