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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875179Generated: October 31, 2026

Cyanogen Bromide → 1-ethyl-5-fluoro-1H-1,3-benzodiazol-2-amine

https://huagongshe.com/reaction/875179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantAmmonium HydroxideHCID 14923—
ReactantN~1~-Ethyl-4-fluorobenzene-1,2-diamineHCID 21286303—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-ethyl-5-fluoro-1H-1,3-benzodiazol-2-amineHCID 43661572—

Reaction Steps

To a solution of N1-ethyl-4-fluoro-benzene-1,2-diamine (1.54 g, 10.0 mmol) in MeOH (20 mL) and H2O (20 mL) was added cyanogen bromide (2.1 mL, 10.5 mmol, 5.0 M in acetonitrile). The resulting mixture was stirred at room temperature over night. The resulting mixture was then adjusted to pH>9 with coned NH4OH and the resulting solid was collected by filtration, washed with H2O and hexanes to yield 1-ethyl-5-fluoro-1H-benzimidazol-2-ylamine MS 180 (M+1)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981113B2
Source datasetuspto-grants-2015_03
ORD IDord-94d5b85c5c3e4b639eaa2062d88fba0e
Source noteuspto-grants-2015_03