Reacción #619088
ord-49fcc1b689bc4e04b52765cb7527cbce
Ecuación de reacción
N-bromosuccinimide
dicyclohexylamine
(2-amino-4-thiazolyl)acetic acid ethyl ester
acetic acid
→
title compound
[5-Bromo-2-(3,3-dicyclohexyl-ureido)-thiazol-4-yl]-acetic acid ethyl ester
[2-(3,3-Dicyclohexyl-ureido)-thiazol-4-yl]-acetic acid ethyl ester
Reactantes
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1ConcentraciónThe reaction mixture was concentrated in vacuo
- 2workup.DISSOLUTIONredissolved in dichloromethane
- 3Lavadowashed with 10% sodium sulphate, water, aqueous sodium bicarbonate, brine
- 4Secadodried over magnesium sulphate
Procedimiento
[2-(3,3-Dicyclohexyl-ureido)-thiazol-4-yl]-acetic acid ethyl ester was prepared from dicyclohexylamine and (2-amino-4-thiazolyl)acetic acid ethyl ester as described in general procedure (A). To this compound was added 1.3 equivalents of N-bromosuccinimide suspended in acetic acid, and the mixture was stirred for 3 h at RT. The reaction mixture was concentrated in vacuo, redissolved in dichloromethane, washed with 10% sodium sulphate, water, aqueous sodium bicarbonate, brine and then dried over magnesium sulphate. Flash chromatography afforded the title compound.