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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465436Generated: October 27, 2026

Ammonium Chloride → 5-Chloropyrazinamide

https://huagongshe.com/reaction/1465436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 5-chloropyrazine-2-carboxylateHCID 406081—
ReactantSodium BicarbonateHCID 516892—
ReactantTrimethylaluminium tolueneHCID 18425018—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product5-ChloropyrazinamideHCID 18145043%

Reaction Conditions

Temperature50 °C

Reaction Steps

Ammonium chloride (558 mg, 10.4 mmol) was suspended in benzene (5 ml) and 2M-trimethylaluminum toluene solution (5.2 ml, 10.4 mmol) was added dropwise at 0° C. After stirring for 1 hr, a solution of methyl 5-chloropyrazine-2-carboxylate (600 mg, 3.48 mmol) in benzene (5 ml) was added. The reaction mixture was heated to 50° C., and stirred overnight. After cooling, the reaction mixture was poured into water, and neutralized with saturated aqueous sodium hydrogen carbonate solution. The mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (dichloromethane:methanol=100:0→98:2) to give 5-chloropyrazine-2-carboxamide (236 mg, yield 43%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999989B2
Source datasetuspto-grants-2015_04
ORD IDord-e204a0d750cf4c0dbf51508a02fad1eb
Source noteuspto-grants-2015_04