Ammonia → Cyclopropyl(4-(trifluoromethyl)phenyl)methanamine
Reaction equation
[CH:1]1([C:4]([C:6]2[CH:11]=[CH:10][C:9]([C:12]([F:15])([F:14])[F:13])=[CH:8][CH:7]=2)=O)[CH2:3][CH2:2]1.[NH3:16]>>[CH:1]1([CH:4]([C:6]2[CH:11]=[CH:10][C:9]([C:12]([F:15])([F:14])[F:13])=[CH:8][CH:7]=2)[NH2:16])[CH2:3][CH2:2]1Participants
3
Procedure
The title compound was prepared using the product from Example 141B and the procedures described in Examples 136A and 136B. 1H NMR (300 MHz, d6-DMSO) 7.92 (m, 4H), 3.24 (d, 1H), 1.92 (broad s, 2H), 0.93 (m, 1H), 0.50-0.27 (m, 4H); MS (DCI/NH3) m/e. 216 (M+H)+.
Sources & evidence
- ORD record
- ord-4deb2a6e67e047b99ea003ecafaf0e8b
- Source dataset
- uspto-grants-2008_02
- Patent number
- US07335678B2
Reaction notes
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