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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849773Generated: October 27, 2026

Triethylamine → N'-t-butyl-N-benzoyl-N'-nicotinoylhydrazine

https://huagongshe.com/reaction/849773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Pyridinecarbonyl chloride, hydrochloride (1:1)HCID 88438—
ReactantN'-tert-butylbenzohydrazideHCID 299436—
SolventDichloromethaneHCID 6344—
ProductN'-t-butyl-N-benzoyl-N'-nicotinoylhydrazineHCID 15767543—

Reaction Conditions

Temperature23 °C

Reaction Steps

A solution of N'-t-butyl-N-benzoylhydrazine (2.0 g) and nicotinoyl chloride hydrochloride in 20 ml of methylene chloride at 23° C. was treated dropwise with triethylamine (4 ml). The reaction mixture was stirred at 23° C. for 0.5 hours. Solids were removed by filtration. The filtrate was diluted with 10N HCl and ether. The layers were separated and the organic layer was washed with 10N HCl. The aqueous layer was neutralized with solid sodium bicarbonate and extracted with ether. The ether extracts were treated with charcoal and then dried with magnesium sulfate. Evaporation of solvents afforded a yellow oil which was chromatographed on silica gel using as eluant a mixture of 10% CH3OH, 40% CH2Cl2, 50% Et2O to afford N'-t-butyl-N-benzoyl-N'-nicotinoylhydrazine as a yellow foam. m.p. 60-63° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06013836
Source datasetuspto-grants-2000_01
ORD IDord-cbc2c9b4c2824e14bc58ad387cff5e02
Source noteuspto-grants-2000_01