Reaction equation
C([N:14]1[CH2:17][CH:16]([O:18][CH:19]([C:31]2[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][CH:32]=2)[C:20]2[CH:25]=[CH:24][C:23]([F:26])=[CH:22][C:21]=2[C:27]([F:30])([F:29])[F:28])[CH2:15]1)(C1C=CC=CC=1)C1C=CC=CC=1.Cl.ClC1C=CC=CC=1C(OC1CNC1)C1C=CC(Cl)=CC=1>>[ClH:37].[F:30][C:27]([F:28])([F:29])[C:21]1[CH:22]=[C:23]([F:26])[CH:24]=[CH:25][C:20]=1[CH:19]([O:18][CH:16]1[CH2:17][NH:14][CH2:15]1)[C:31]1[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][CH:32]=1Participants
3
Procedure
This material was prepared from 1-benzhydryl-3-[2-(trifluoromethyl)-4-fluoro-4′-chlorobenzhydryloxy]azetidine (124) (3.8 mmol) using the procedure described for compound (9) (1.45 g, 97%).
Sources & evidence
- ORD record
- ord-c98931b763da4f8aaff60b5608364577
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07504522B2
Linked notes
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