Reaktion #1905469

ord-8edbf3d0f2014a7bb466b7286dc0f3f1

Reaktionsgleichung

CC1CCC(N(C(=O)Nc2ncc(Br)s2)C2CCOCC2)CC1
3-(5-bromo-thiazol-2-yl)-1-(4-methylcyclohexyl)-1-(tetrahydro-pyran-4-yl)-urea
CC1CCC(N(C(=O)Nc2ncc(Br)s2)C2CCOCC2)CC1
3-(5-Bromo-thiazol-2-yl)-1-(4-methyl-cyclohexyl)-1-(tetrahydro-pyran-4-yl)-urea
CCOC(=O)c1cnc(S)n1C
2-mercapto-3-methyl-3H-imidazole-4-carboxylic acid ethyl ester
→
CCOC(=O)c1cnc(Sc2cnc(NC(=O)N(C3CCOCC3)C3CCC(C)CC3)s2)n1C
3-Methyl-2-{2-[3-(4-methyl-cyclohexyl)-3-(tetrahydro-pyran-4-yl)-ureido]-thiazol-5-ylsulfanyl}-3H-imidazole-4-carboxylic acid ethyl ester

Edukte

CC1CCC(N(C(=O)Nc2ncc(Br)s2)C2CCOCC2)CC1
3-(5-bromo-thiazol-2-yl)-1-(4-methylcyclohexyl)-1-(tetrahydro-pyran-4-yl)-urea
CC1CCC(N(C(=O)Nc2ncc(Br)s2)C2CCOCC2)CC1
3-(5-Bromo-thiazol-2-yl)-1-(4-methyl-cyclohexyl)-1-(tetrahydro-pyran-4-yl)-urea
CCOC(=O)c1cnc(S)n1C
2-mercapto-3-methyl-3H-imidazole-4-carboxylic acid ethyl ester

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigePrepared

Vorschrift

Prepared as described in general procedure (E) using 3-(5-bromo-thiazol-2-yl)-1-(4-methylcyclohexyl)-1-(tetrahydro-pyran-4-yl)-urea (Example 203) and 2-mercapto-3-methyl-3H-imidazole-4-carboxylic acid ethyl ester.

Quelle

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