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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356393Generated: October 25, 2026

Dimethylformamide → 6-chloro-N-(3-methylbutyl)pyridazine-3-carboxamide

https://huagongshe.com/reaction/2356393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantIsoamylamineHCID 7894—
ReactantThionyl ChlorideHCID 24386—
Reactant6-Hydroxy-3-pyridazinecarboxylic acid monohydrateHCID 2774651—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product6-chloro-N-(3-methylbutyl)pyridazine-3-carboxamideHCID 1673378698%

Reaction Steps

The mixture of 6-oxo-1,6-dihydropyridazine-3-carboxylic acid monohydrate (3.16 g; 20.0 mmol), dimethylformamide (0.5 mL) and thionyl chloride (5-7 mL) in chloroform (70 mL) was kept at 50-60° C. overnight. The reaction mixture was evaporated in vacuo to dryness. The solid residue was dissolved in dichloromethane (70 mL) and added dropwise to the mixture of 3-methylbutylamine (30 mmol, 2.7 mL) and triethylamine (5 mL) in dichloromethane (150 mL) at ambient temperature. The mixture was stirred for 30 min, washed sequentially with 10% HCl solution, saturated NaHCO3 and water, and then dried over MgSO4. The final compound was isolated by recrystallization from ether-hexanes (5:1) (19.76 mmol). Yield: 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759348B2
Source datasetuspto-grants-2010_07
ORD IDord-dd645fbdb4fb4c2f937184fae8e86d8f
Source noteuspto-grants-2010_07