Reaktion #358095

ord-1c927c9562ff4949be1444ac8ecf3e6e

Reaktionsgleichung

CN(C)C=O
DMF
Fc1cccc(-c2[nH]nc(C(F)(F)F)c2Cl)c1
4-Chloro-5-[3-Fluorophenyl]-3-trifluoromethyl-1H-pyrazole
O=C([O-])[O-].[K+].[K+]
K2CO3
COc1cc(N2CCN(C(=O)CCl)CC2)ccc1Cl
2-Chloro-1-[4-(4-chloro-3-methoxy-phenyl)-piperazin-1-yl]-ethanone
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3cccc(F)c3)CC2)ccc1Cl
title compound
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3cccc(F)c3)CC2)ccc1Cl
1-[4-(4-Chloro-3-methoxyphenyl)-piperazin-1-yl]-2-(4-chloro-5-[3-Fluoro-phenyl]-3-trifluoromethyl-pyrazol-1-yl)-ethanone

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Protocol T was followed using 4-Chloro-5-[3-Fluorophenyl]-3-trifluoromethyl-1H-pyrazole, K2CO3, 2-Chloro-1-[4-(4-chloro-3-methoxy-phenyl)-piperazin-1-yl]-ethanone and DMF. Column chromatography using a solvent mixture (hexane/ethyl acetate=2/3, Rf=0.59) afforded the title compound as a white solid. 1H NMR (400 MHz, CDCl3): 7.64-7.68 (d, 1H), 7.56-7.62 (d, 1H), 7.36-7.42 (m, 1H), 7.22-7.24 (m, 2H), 7.08-7.12 (m, 1H), 6.42-6.52 (m, 2H), 5.2 (s, 2H), 3.9 (s, 3H), 3.62-3.82 (m, 4H), 3.12-3.22 (m, 4H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07449576B1uspto-grants-2008_11