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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251180Generated: November 3, 2026

Hydrogen Bromide → 4-Bromothieno[3,2-C]pyridin-6-amine

https://huagongshe.com/reaction/1251180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium HydroxideHCID 14798—
Reactant2-(Cyanomethyl)thiophene-3-carbonitrileHCID 22503439—
SolventAcetic AcidHCID 176—
Product4-Bromothieno[3,2-C]pyridin-6-amineHCID 2250342370%

Reaction Steps

2-Cyanomethyl-3-cyanothiophene (823 mg) was added to a solution (30 ml) of 25% hydrogen bromide in acetic acid, and the resulting mixture was stirred under ice-cooling for 90 min, which was neutralized with a 8N aqueous solution of sodium hydroxide and then extracted with ethyl acetate. The organic layer was washed with water, dried (over MgSO4) and evaporated. The residue was purified by silica gel column chromatography (ethyl acetate/hexane system), to give the title compound as a yellow solid (894 mg, yield; 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340759B1
Source datasetuspto-grants-2002_01
ORD IDord-2623786af7d6425c94c505bb58e434d5
Source noteuspto-grants-2002_01