1-(Bromomethyl)-2-chloro-4-fluorobenzene → 1-(2-Chloro-4-fluorobenzyl)-2-cyclooctyl-4,4-dimethyl-1,2-diazetidin-3-one

HRID 888832Notes

Reaction equation

HRID 888832 reaction equation
[CH:1]1([N:9]2[C:12](=[O:13])[C:11]([CH3:15])([CH3:14])[NH:10]2)[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:16][C:17]1[CH:24]=[C:23]([F:25])[CH:22]=[CH:21][C:18]=1[CH2:19]Br>>[Cl:16][C:17]1[CH:24]=[C:23]([F:25])[CH:22]=[CH:21][C:18]=1[CH2:19][N:10]1[C:11]([CH3:15])([CH3:14])[C:12](=[O:13])[N:9]1[CH:1]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

3

Reactant 2

HCID 27250621-(Bromomethyl)-2-chloro-4-fluorobenzeneHCID 673029832-Cyclooctyl-4,4-dimethyl-1,2-diazetidin-3-one

Product 1

HCID 593613981-(2-Chloro-4-fluorobenzyl)-2-cyclooctyl-4,4-dimethyl-1,2-diazetidin-3-one

Procedure

2-Cyclooctyl-4,4-dimethyl-1,2-diazetidin-3-one and 2-chloro-4-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 crystalline powder.

Sources & evidence

ORD record
ord-3756b5694dea4eef87ed49b4a2f5de74
Source dataset
uspto-grants-2012_08
Patent number
US08252781B2

Reaction notes

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