2'-Aminoacetophenone → N-(2-Acetylphenyl)cyclohexanecarboxamide
Reaction equation
FC(F)(F)C1C=CC=CC=1N[C:10]([CH:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1)=[O:11].[C:20]([C:23]1[CH:29]=[CH:28][CH:27]=[CH:26][C:24]=1[NH2:25])(=[O:22])[CH3:21]>>[C:20]([C:23]1[CH:29]=[CH:28][CH:27]=[CH:26][C:24]=1[NH:25][C:10]([CH:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1)=[O:11])(=[O:22])[CH3:21]Participants
3
Procedure
This compound was prepared following the procedure described for compound 26A of example 26, except that 2-acetylaniline was used in place of 2-trifluoromethylaniline. Yield: 90%.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-f7975d14192442a39efe95a2f63c63fa
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06399614B1
Reaction notes
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