3-(4-tert-Butylphenyl)-3-chloro-1-(diphenylmethyl)azetidine → 3-Chloro-3-(4-(trifluoromethyl)phenyl)(dipbenylmethyl)azetidine
Reaction equation
[F:1][C:2]([F:28])([F:27])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2(O)[CH2:12][N:11]([CH:13]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH2:10]2)=[CH:5][CH:4]=1.C(C1C=CC(C2([Cl:56])CN(C(C3C=CC=CC=3)C3C=CC=CC=3)C2)=CC=1)(C)(C)C>>[Cl:56][C:9]1([C:6]2[CH:7]=[CH:8][C:3]([C:2]([F:28])([F:27])[F:1])=[CH:4][CH:5]=2)[CH2:12][N:11]([CH:13]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:10]1Participants
3
Procedure
This compound was prepared from compound (30) using the procedure described for compound (10).
Sources & evidence
- ORD record
- ord-141bbe1872cd45419de15fca81555ecb
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06831078B1
Reaction notes
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