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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606527Generated: November 1, 2026

Cyanogen Bromide → HCID 21543672, compound

https://huagongshe.com/reaction/1606527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantQuinoline, 2-hydrazinyl-HCID 85111—
SolventMethanolHCID 887—
ProductHCID 21543672HCID 21543672—

Reaction Steps

2-Hydrazinoquinoline (25.0 grams) was placed in a 3-liter flask (three-necked, equipped with a condenser) containing 1500 milliliters of methanol. To this flask was added 17 grams of cyanogen bromide. The reaction mixture was refluxed for six hours, at which time it was cooled. The reaction mixture was then evaporated down to approximately 200 milliliters. This solution was then poured into 1 liter of absolute ether. The precipitate which formed was washed with an aliphatic naphtha solvent. This precipitate, the desired 1 -amino-s-triazolo(4,3-a)quinoline hydrobromide, was separated by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953457
Source datasetuspto-grants-1976_04
ORD IDord-eb82cfe6bf6148128cddf3d8098c9086
Source noteuspto-grants-1976_04