Reaktion #340993

ord-53ed6886296d45d1be24285f3568254a

Reaktionsgleichung

CI
methyliodide
CCCC(=O)N1CCC(N(C(=O)Nc2ncc(SC#N)s2)C2CCC(C)CC2)CC1
1-(1-butyryl-piperidin-4-yl)-1-(4-methyl-cyclohexyl)-3-(5-thiocyanato-thiazol-2-yl)-urea
O[C@H](CS)[C@@H](O)CS
dithioerythritol
→
CCCC(=O)N1CCC(N(C(=O)Nc2ncc(SC)s2)C2CCCCC2)CC1
1-(1-Butyryl-piperidin-4-yl)-1-cyclohexyl-3-(5-methylsulfanyl-thiazol-2-yl)-urea

Edukte

CI
methyliodide
—
( I )
CCCC(=O)N1CCC(N(C(=O)Nc2ncc(SC#N)s2)C2CCC(C)CC2)CC1
1-(1-butyryl-piperidin-4-yl)-1-(4-methyl-cyclohexyl)-3-(5-thiocyanato-thiazol-2-yl)-urea
O[C@H](CS)[C@@H](O)CS
dithioerythritol

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigePrepared

Vorschrift

Prepared as described in general procedure (H) and (I) using 1-(1-butyryl-piperidin-4-yl)-1-(4-methyl-cyclohexyl)-3-(5-thiocyanato-thiazol-2-yl)-urea, dithioerythritol and methyliodide.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07872139B2uspto-grants-2011_01