Hydroxyamine hydrochloride → HCID 89691114, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[N:9]=[C:8]([CH:10]3[CH2:13][CH:12]([CH:14]=O)[CH2:11]3)[N:7]([CH3:16])[C:6]=2[CH:17]=1.Cl.[NH2:19][OH:20]>CCO>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[N:9]=[C:8]([CH:10]3[CH2:13][CH:12]([CH:14]=[N:19][OH:20])[CH2:11]3)[N:7]([CH3:16])[C:6]=2[CH:17]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of 3-(6-bromo-1-methyl-1H-benzimidazol-2-yl)cyclobutanecarbaldehyde (less polar isomer, 200 mg) in EtOH (10 ml) was added hydroxylamine hydrochloride (50 mg), and the resulting mixture was heated under reflux for 2 h. The reaction mixture was concentrated in vacuo to afford the title compound (200 mg) as an off-white solid.
Workup
- temperaturethe resulting mixture was heated
- temperatureunder reflux for 2 h
- concentrationThe reaction mixture was concentrated in vacuo
Sources & evidence
- ORD record
- ord-5ec8024fed5c4231b54b47faa6811c53
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09365540B2
Reaction notes
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