4-(Trifluoromethyl)benzenesulfonamide → N-[({2-[4-(3,5-Dimethyl-4-phenyl-1H-pyrazol-1-yl)phenyl]ethyl}amino)carbonyl]-4-(trifluoromethyl)benzenesulfonamide

HRID 891093

反応式

HRID 891093 の反応式
[CH3:1][C:2]1[C:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[C:5]([CH3:13])[N:4]([C:14]2[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][NH:22][C:23](=O)[O:24]C3C=CC=CC=3)=[CH:16][CH:15]=2)[N:3]=1.[F:32][C:33]([F:45])([F:44])[C:34]1[CH:39]=[CH:38][C:37]([S:40]([NH2:43])(=[O:42])=[O:41])=[CH:36][CH:35]=1>>[CH3:1][C:2]1[C:6]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)=[C:5]([CH3:13])[N:4]([C:14]2[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][NH:22][C:23]([NH:43][S:40]([C:37]3[CH:36]=[CH:35][C:34]([C:33]([F:32])([F:45])[F:44])=[CH:39][CH:38]=3)(=[O:41])=[O:42])=[O:24])=[CH:16][CH:15]=2)[N:3]=1

参加物

3

反応物 2

HCID 700184-(Trifluoromethyl)benzenesulfonamideHCID 22244550Phenyl 2-[4-(3,5-dimethyl-4-phenyl-1H-pyrazol-1-yl)phenyl]ethylcarbamate

生成物 1

HCID 22244534N-[({2-[4-(3,5-Dimethyl-4-phenyl-1H-pyrazol-1-yl)phenyl]ethyl}amino)carbonyl]-4-(trifluoromethyl)benzenesulfonamide

実験手順

The title compound was prepared according to the procedure described in step 2 of Example 22 from phenyl 2-[4-(3,5-dimethyl-4-phenyl-1H-pyrazol-1-yl)phenyl]ethylcarbamate (step 1 of Example 22) and 4-(trifluoromethyl)benzenesulfonamide: 1H-NMR (CDCl3) δ 8.06 (2H, d, J=7.7 Hz), 7.80 (2H, d, J=8.2 Hz), 7.47-7.21 (9H, m), 6.10 (1H, br.s), 3.50-3.43 (2H, m), 2.86 (2H, t, J=6.3 Hz), 2.32 (3H, s), 2.23 (3H, s).

出典と根拠

ORDレコード
ord-2a94aba85be3483385a5919f87aa30a7
出典データセット
uspto-grants-2006_02
特許番号
US07001917B2

関連ノート

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