Benzimidazole → 1H-benzimidazol-1-ylacetonitrile
Reaction equation
[N:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[NH:3][CH:2]=1.Br[CH2:11][C:12]#[N:13]>>[N:1]1([CH2:11][C:12]#[N:13])[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1Participants
3
Procedure
The title compound is synthesized by coupling of Benzimidazole and bromoacetonitrile analogously to the preparation of Intermediate 149.2 as a colorless solid; ES-MS: M+H=158.0: CtRet=3.42.
Sources & evidence
- ORD record
- ord-94050b9383184e16b1c38fcaa60d520e
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08053457B2
Reaction notes
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