4-(Trifluoromethoxy)aniline → HCID 51001732, compound
Reaction equation
[F:1][C:2]1([C:21]([OH:23])=O)[CH2:7][CH2:6][N:5]([S:8]([C:11]2[C:12]([C:17]([F:20])([F:19])[F:18])=[N:13][N:14]([CH3:16])[CH:15]=2)(=[O:10])=[O:9])[CH2:4][CH2:3]1.[F:24][C:25]([F:35])([F:34])[O:26][C:27]1[CH:33]=[CH:32][C:30]([NH2:31])=[CH:29][CH:28]=1>>[F:24][C:25]([F:34])([F:35])[O:26][C:27]1[CH:28]=[CH:29][C:30]([NH:31][C:21]([C:2]2([F:1])[CH2:3][CH2:4][N:5]([S:8]([C:11]3[C:12]([C:17]([F:18])([F:19])[F:20])=[N:13][N:14]([CH3:16])[CH:15]=3)(=[O:9])=[O:10])[CH2:6][CH2:7]2)=[O:23])=[CH:32][CH:33]=1Participants
3
Procedure
This material was made in analogy to example 1 from 4-fluoro-1-(1-methyl-3-trifluoromethyl-1H-pyrazole-4-sulfonyl)-piperidine-4-carboxylic acid (0.176 g) and 4-trifluoromethoxy-aniline (0.087 g) to give the desired 4-fluoro-1-(1-methyl-3-trifluoromethyl-1H-pyrazole-4-sulfonyl)-piperidine-4-carboxylic acid (4-trifluoromethoxy-phenyl)-amide (0.04 g) as a white solid. MS (ESI): 519.28 (MH+).
Sources & evidence
- ORD record
- ord-2587259bcd8a438f995a04f6709683ce
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08258158B2
Reaction notes
Loading…