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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525511Generated: November 3, 2026

Cyanogen Bromide → HCID 178422405, compound

https://huagongshe.com/reaction/1525511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 178422411HCID 178422411—
SolventMethanolHCID 887—
ProductHCID 178422405HCID 178422405101.2%

Reaction Steps

7-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]imidazol-2-amine 3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,2-diamine (See Example 1.G) (500 mg, 2.015 mmol) and cyanic bromide (0.484 mL, 2.418 mmol) were added to a round bottom flask at room temperature, suspended in methanol (10.0 mL) and allowed to stir for 1.5 h. Volatiles were removed under reduced pressure followed by the addition of saturated sodium bicarbonate. The precipitate was collected via filtration, washed with ethyl acetate and dried under reduced pressure to afford the title compound (557 mg, 2.039 mmol, quant. yield). Compound was carried forward without further purification or characterization. MS (ESI) m/z 273.8 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079900B2
Source datasetuspto-grants-2015_07
ORD IDord-68ed35701596488fbab087b6202bd571
Source noteuspto-grants-2015_07