3-Chloro-3-(3-(trifluoromethyl)phenyl)-(diphenylmethyl)azetidine → 3-(3-(Trifluoromethyl)phenyl)-1-(diphenylmethyl)azetidine
Reaction equation
Cl[C:2]1([C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([C:25]([F:28])([F:27])[F:26])[CH:20]=2)[CH2:5][N:4]([CH:6]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH2:3]1.C(C1C=CC(C2CCN2C(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1)(C)(C)C>>[F:28][C:25]([F:26])([F:27])[C:21]1[CH:20]=[C:19]([CH:2]2[CH2:3][N:4]([CH:6]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:7]3[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=3)[CH2:5]2)[CH:24]=[CH:23][CH:22]=1Participants
3
Procedure
This compound was prepared compound (37) using the procedure described for compound (11).
Sources & evidence
- ORD record
- ord-d1202ea486c548c1b7d94746b735fc76
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06831078B1
Reaction notes
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