2-Chloro-5-fluorobenzyl bromide → HCID 67303381, compound

HRID 888844Notes

Reaction equation

HRID 888844 reaction equation
[CH:1]1([N:8]2[C:11](=[O:12])[C:10]([CH3:14])([CH3:13])[NH:9]2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:15][C:16]1[CH:23]=[CH:22][C:21]([F:24])=[CH:20][C:17]=1[CH2:18]Br>>[Cl:15][C:16]1[CH:23]=[CH:22][C:21]([F:24])=[CH:20][C:17]=1[CH2:18][N:9]1[C:10]([CH3:14])([CH3:13])[C:11](=[O:12])[N:8]1[CH:1]1[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]1

Participants

3

Reactant 2

HCID 27736232-Chloro-5-fluorobenzyl bromideHCID 67303075HCID 67303075, compound

Product 1

HCID 67303381HCID 67303381, compound

Procedure

2-Cycloheptyl-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-87cde29bccec4302a5f2cf3f6424c838
Source dataset
uspto-grants-2012_08
Patent number
US08252781B2

Reaction notes

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