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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541410Generated: November 2, 2026

Isoniazid → N-(5-(4-(4-Cyanophenyl)piperidine-1-carbonyl)-2-methylphenyl)-2-isonicotinoylhydrazinecarboxamide

https://huagongshe.com/reaction/541410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoniazidHCID 3767—
ReactantPhosgeneHCID 6371—
ReactantTriethylamineHCID 8471—
Reactant4-(1-(3-Amino-4-methylbenzoyl)piperidin-4-yl)benzonitrileHCID 57666915—
SolventDichloromethaneHCID 6344—
ProductN-(5-(4-(4-Cyanophenyl)piperidine-1-carbonyl)-2-methylphenyl)-2-isonicotinoylhydrazinecarboxamideHCID 68288800—

Reaction Steps

A solution of 4-(1-(3-Amino-4-methylbenzoyl)piperidin-4-yl)benzonitrile (compound 121.1, 0.1 g, 0.31 mmol) and triethyl amine (0.09 ml, 0.62 mmol) in DCM (5 ml) was added to a solution of phosgene (20% in toluene, 0.31 ml, 0.62 mmol) in DCM (5 ml) at 0° C. After the resulting reaction mixture was stirred at room temperature for 1.5 hours, all solvents were removed under reduced pressure. The residue was dried under high-vacuum for 30 minutes then was re-dissolved in EtOH (5 ml). Isonicotinohydrazide (0.05 g, 0.34 mmol) was added. The mixture was heated at 80° C. over night. The ethanol was removed and the residue was purified using prep.-TLC (10% MeOH in DCM) to give the product as a light brown solid. Yield: 0.14 g, 93%. m/z (ES+) 483.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-e7134e189a0e40148226645e3d6d3836
Source noteuspto-grants-2014_10