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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787549Generated: October 29, 2026

Cyanogen Bromide → HCID 178419694, compound

https://huagongshe.com/reaction/1787549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 10931743HCID 10931743—
SolventMethanolHCID 887—
ProductHCID 178419694HCID 17841969460%

Reaction Steps

To a suspension of 2-(4,5-dihydro-1H-imidazol-2-yl)aniline (5.00 g, 31.0 mmol) in 85% methanol (60 ml) at 0° C. was added cyanogen bromide (3.61 g, 34.1 mmol) by portions. This mixture was stirred at room temperature overnight. After the mixture was concentrated under reduced pressure, the resulting precipitate was collected by filtration. This pale green solid was washed with water, methanol and diethyl ether successively, and dried under reduced pressure to give 2,3-dihydroimidazo[1,2-c]quinazolin-5-ylamine hydrobromide (4.94 g, 60% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511041B2
Source datasetuspto-grants-2009_03
ORD IDord-98b2241b8f4840818d172daa293a975c
Source noteuspto-grants-2009_03