Reacción #619196

ord-321e26b7602e47398405104d506cb837

Ecuación de reacción

CCOC(=O)C(C)Sc1cnc(NC(=O)N(C2CCCCCC2)C2CCCC2)s1
[2-(3-Cycloheptyl-3-cyclopentyl-ureido)-thiazol-5-ylsulfanyl]-propionic acid ethyl ester
C1CCCC(NC2CCCC2)CC1
cycloheptyl-cyclopentylamine
CCOC(=O)CS.Nc1cncs1
5-aminothiazole 2-mercaptoacetic acid ethyl ester
→
O=C(O)CCSc1cnc(NC(=O)N(C2CCCCCC2)C2CCCC2)s1
title compound
O=C(O)CCSc1cnc(NC(=O)N(C2CCCCCC2)C2CCCC2)s1
3-[2-(3-Cycloheptyl-3-cyclopentyl-ureido)-thiazol-5-ylsulfanyl]-propionic acid

Reactantes

CCOC(=O)C(C)Sc1cnc(NC(=O)N(C2CCCCCC2)C2CCCC2)s1
[2-(3-Cycloheptyl-3-cyclopentyl-ureido)-thiazol-5-ylsulfanyl]-propionic acid ethyl ester
C1CCCC(NC2CCCC2)CC1
cycloheptyl-cyclopentylamine
CCOC(=O)CS.Nc1cncs1
5-aminothiazole 2-mercaptoacetic acid ethyl ester

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroHydrolysis

Procedimiento

[2-(3-Cycloheptyl-3-cyclopentyl-ureido)-thiazol-5-ylsulfanyl]-propionic acid ethyl ester pre-pared as described in general procedure (A) using cycloheptyl-cyclopentylamine and 5-aminothiazole-2-mercaptoacetic acid ethyl ester. Hydrolysis using general procedure (F) gave the title compound

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE045183E1uspto-grants-2014_10