2-(Trifluoromethyl)benzoyl chloride → HCID 69353843, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][CH:16]=1)[C:5]([CH:7]1[CH2:12][CH2:11][N:10]([CH3:13])[CH2:9][CH2:8]1)=[O:6].[F:17][C:18]([F:29])([F:28])[C:19]1[CH:27]=[CH:26][CH:25]=[CH:24][C:20]=1[C:21](Cl)=[O:22]>>[F:17][C:18]([F:28])([F:29])[C:19]1[CH:27]=[CH:26][CH:25]=[CH:24][C:20]=1[C:21]([NH:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][CH:16]=1)[C:5]([CH:7]1[CH2:8][CH2:9][N:10]([CH3:13])[CH2:11][CH2:12]1)=[O:6])=[O:22]Participants
3
Procedure
Beginning with 4-[3-aminobenzoyl]-1-methylpiperidine (50 mg, 0.229 mmol) and 2-(trifluoromethyl)benzoyl chloride (101 μl, 0.687 mmol), 81.9 mg (92%) of the title compound were recovered.
Sources & evidence
- ORD record
- ord-fe36e771856a41adbe83e4e6d63a44a2
- Source dataset
- uspto-grants-2004_08
- Patent number
- US06777428B1
Reaction notes
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