Reaktion #469163

ord-085d61e57cf0434b898ce70ed81dc903

Reaktionsgleichung

CS(=O)(=O)c1ccc(-c2cn[nH]c(=O)c2-c2ccc(F)c(F)c2)cc1
4-(3,4-difluorophenyl)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone
Fc1ccc(Br)cc1F
3,4-difluorobromobenzene
N
NH3
CS(=O)(=O)c1ccc(-c2cnn(-c3ccc(F)c(F)c3)c(=O)c2-c2cccc(F)c2)cc1
title compound
CS(=O)(=O)c1ccc(-c2cnn(-c3ccc(F)c(F)c3)c(=O)c2-c2cccc(F)c2)cc1
2-(3,4-Difluorophenyl)-4-(3-fluorophenyl)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The title compound was prepared as described in Example 62, starting with 4-(3,4-difluorophenyl)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone in place of 4-(4-fluorophenyl)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone and substituting 3,4-difluorobromobenzene in place of 1-bromo-4-fluorobenzene (yield: 185 mg, 46.5%). mp 182-185° C. 1H NMR (300 MHz, DMSO-d6) δ 3.23 (s, 3H), 6.98 (d, J=9 Hz, 1H), 7.18 (m, 2H), 7.32 (m, 1H), 7.52 (d, J=9 Hz, 2 H), 7.6 (m, 2H), 7.85 (m, 1H), 7.9 (d, J=9 Hz, 2H), 8.3 (s, 1H). MS (DCI/NH3) m/z 457 (M+H)+, 474 (M+NH4)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06307047B1uspto-grants-2001_10