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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21653Generated: October 29, 2026

2-Pyrazinecarboxylic acid → N'-t-butyl-N-(pyrazinecarbonyl)-N'benzoylhydrazine

https://huagongshe.com/reaction/21653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Pyrazinecarboxylic acidHCID 1047—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(tert-butyl)benzohydrazideHCID 1275961—
SolventDichloromethaneHCID 6344—
ProductN'-t-butyl-N-(pyrazinecarbonyl)-N'benzoylhydrazineHCID 15767548—

Reaction Conditions

Temperature23 °C

Reaction Steps

Triethylamine (1.0 g, 0.01 mol) was added to a solution of N'-t-butyl-N'-benzoylhydrazine (0.86 g, 0.0031 mol) and pyrazine carboxylic acid (0.56 g, 0.0045 mol) in 10 ml of methylene chloride at 23° C. This mixture was added to a solution of methanesulfonyl chloride (0.6 g, 0.0052 mol) in 10 ml of methylene chloride at 0° C. The mixture was stirred at 23° C. for 3 hours and then allowed to stand at 23° C. overnight. Aqueous sodium bicarbonate was added and the layers were separated. The organic extracts were evaporated to give crude product which was triturated with ether to afford N'-t-butyl-N-(pyrazinecarbonyl)-N'-benzoylhydrazine as a white solid: m.p. 181°-183° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424333
Source datasetuspto-grants-1995_06
ORD IDord-ec7670aeb74047e3932a8754f3a46ae4
Source noteuspto-grants-1995_06