Reaktion #1905474

ord-6f4c430e335244d597d4459f26c609f7

Reaktionsgleichung

O=C(Nc1nc(CBr)cs1)N(C1CCCCC1)C1CCCCC1
1,1-dicyclohexyl-3-(4-bromomethyl-thiazol-2-yl)urea
CCOC(=O)c1c[nH]c(S)n1
2-mercapto-1H-imidazole-4-carboxylic acid ethyl ester
→
CCOC(=O)c1c[nH]c(SCc2csc(NC(=O)N(C3CCCCC3)C3CCCCC3)n2)n1
2-[2-(3,3-Dicyclohexylureido)-thiazol-4-ylmethylsulfanyl)-1H-imidazole-4-carboxylic acid ethyl ester
Ausbeute 20.0%

Edukte

O=C(Nc1nc(CBr)cs1)N(C1CCCCC1)C1CCCCC1
1,1-dicyclohexyl-3-(4-bromomethyl-thiazol-2-yl)urea
CCOC(=O)c1c[nH]c(S)n1
2-mercapto-1H-imidazole-4-carboxylic acid ethyl ester

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigePrepared in 20% yield

Vorschrift

Prepared in 20% yield as described in general procedure (L) from 1,1-dicyclohexyl-3-(4-bromomethyl-thiazol-2-yl)urea and 2-mercapto-1H-imidazole-4-carboxylic acid ethyl ester.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07598391B2uspto-grants-2009_10