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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288608Generated: October 29, 2026

Cyanogen Bromide → HCID 18699937, compound

https://huagongshe.com/reaction/2288608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 55213626HCID 55213626—
SolventEthanolHCID 702—
ProductHCID 18699937HCID 1869993740.7%

Reaction Steps

2.5 g (23.57 mmol) of cyanogen bromide was added to 250 ml of ethanol solution containing 5.43 g (21.43 mmol) of 2-(hexahydro-1H-azepin-1-yl)methylthiophene-5-carboxylic acid hydrazide, and the mixture was stirred at room temperature for 2 hours and then at 50° C. for 7 hours. The reaction solution was concentrated under a reduced pressure, saturated sodium bicarbonate aqueous solution and chloroform were added to the resulting residue. Then, the resulting organic layer was separated, washed with saturated brine and then dried over anhydrous magnesium sulfate. The solvent was evaporated and the resulting residue was recrystallized from ethyl acetate to give 2.43 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090804
Source datasetuspto-grants-2000_07
ORD IDord-b92c754fe7404644b17285bea76c60fc
Source noteuspto-grants-2000_07