HCID 67055305, compound → HCID 86609773, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([C:9](=[C:15]2[CH2:18][N:17]([CH:19]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:16]2)[C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH:5]=[C:6]([F:8])[CH:7]=1>C1COCC1>[Br:1][C:2]1[CH:3]=[C:4]([CH:9]([CH:15]2[CH2:18][N:17]([CH:19]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH2:16]2)[C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH:5]=[C:6]([F:8])[CH:7]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared from ethyl (3-bromo-5-fluorophenyl)[1-(diphenylmethyl) azetidin-3-ylidene]acetate according to the procedure described in Preparation 6 except that THF was used as the co-solvent; Mass Spectrum: m/e=482 (M+1, 79Br), 484 (M+1, 81Br).
Sources & evidence
- ORD record
- ord-87029186b58944cfa4d9d664d2148a89
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07906652B2
Reaction notes
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