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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131113Generated: October 29, 2026

Sulfuric Acid → 4-(2-Methylphenyl)-6-(4-methyl-1-piperazinyl)-3-pyridinecarboxamide

https://huagongshe.com/reaction/131113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
Reactant6-(4-Methyl-piperazin-1-yl)-4-o-tolyl-nicotinonitrileHCID 11380789—
SolventWaterHCID 962—
Product4-(2-Methylphenyl)-6-(4-methyl-1-piperazinyl)-3-pyridinecarboxamideHCID 1148372898.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of crude 5-cyano-4-(2-methylphenyl)-2-(4-methylpiperazinyl) pyridine (16.85 g, 57.6 mmol), 18 mL of toluene, and 27 mL (49.7 g, 507 mmol) of concentrated sulfuric acid was heated at 70° C. for 12 hours. The mixture was cooled and quenched with 200 mL of cold H2O. Ethyl acetate was added followed by a solution of 45.6 g (1.14 mol) of sodium hydroxide in 200 mL of H2O. Water (200 mL) was added and the layers were separated. The aqueous layer was extracted several times with 100 mL of ethyl. The organic layers were combined and concentrated to afford 17.55 g (98.1%) of 4-(2-methylphenyl)-6-(4-methylpiperazinyl)-3-pyridinecarboxamide as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384939B2
Source datasetuspto-grants-2008_06
ORD IDord-37ada9ab5fa84acdbc33e8cae08b2aa0
Source noteuspto-grants-2008_06