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

HRID 891094Notes

Reaction equation

HRID 891094 reaction equation
[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:46])([F:45])[O:34][C:35]1[CH:40]=[CH:39][C:38]([S:41]([NH2:44])(=[O:43])=[O:42])=[CH:37][CH:36]=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:15]=[CH:16][C:17]([CH2:20][CH2:21][NH:22][C:23]([NH:44][S:41]([C:38]3[CH:39]=[CH:40][C:35]([O:34][C:33]([F:32])([F:45])[F:46])=[CH:36][CH:37]=3)(=[O:42])=[O:43])=[O:24])=[CH:18][CH:19]=2)[N:3]=1

Participants

3

Reactant 2

HCID 27772114-(Trifluoromethoxy)benzenesulfonamideHCID 22244550Phenyl 2-[4-(3,5-dimethyl-4-phenyl-1H-pyrazol-1-yl)phenyl]ethylcarbamate

Product 1

HCID 10289728N-[({2-[4-(3,5-Dimethyl-4-phenyl-1H-pyrazol-1-yl)phenyl]ethyl}amino)carbonyl]-4-[(trifluoromethyl)oxy]benzenesulfonamide

Procedure

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)oxy]benzenesulfonamide: 1H-NMR (CDCl3) δ 7.98 (2H, d, J=9.1 Hz), 7.47-7.21 (11H, m), δ 12 (1H, br.s), 3.50-3.43 (2H, m), 2.85 (2H, t, J=6:5 Hz). 2.32 (3H, s), 2.23 (3H, s).

Sources & evidence

ORD record
ord-01f22edab81141a88b0fd128b2f72ae4
Source dataset
uspto-grants-2006_02
Patent number
US07001917B2

Reaction notes

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