2-Chloro-5-fluorobenzyl bromide → 1-(2-Chloro-5-fluorobenzyl)-2-cyclohexyl-4,4-dimethyl-1,2-diazetidin-3-one
Reaction equation
[CH:1]1([N:7]2[C:10](=[O:11])[C:9]([CH3:13])([CH3:12])[NH:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:14][C:15]1[CH:22]=[CH:21][C:20]([F:23])=[CH:19][C:16]=1[CH2:17]Br>>[Cl:14][C:15]1[CH:22]=[CH:21][C:20]([F:23])=[CH:19][C:16]=1[CH2:17][N:8]1[C:9]([CH3:13])([CH3:12])[C:10](=[O:11])[N:7]1[CH:1]1[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1Participants
3
Procedure
2-Cyclohexyl-4,4-dimethyl-1,2-diazetidin-3-one and 2-chloro-5-fluorobenzyl bromide were used for a similar reaction and treatment as Process 6 of Example 1, and the title compound was obtained as a colorless oil.
Sources & evidence
- ORD record
- ord-7b10b8ba01da4e6e8b284c9203c3af18
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252781B2
Reaction notes
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