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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356401Generated: October 25, 2026

Chloroform → 6-CHLOROPYRIDAZINE-3-CARBOXYLIC Acid (2-CYCLOBUTYLETHYL)AMIDE

https://huagongshe.com/reaction/2356401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantThionyl ChlorideHCID 24386—
Reactant6-Hydroxy-3-pyridazinecarboxylic acid monohydrateHCID 2774651—
Reactant2-Cyclobutylethan-1-amineHCID 19017814—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product6-CHLOROPYRIDAZINE-3-CARBOXYLIC Acid (2-CYCLOBUTYLETHYL)AMIDEHCID 8602604559%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a 100-mL round bottom flask, 6-oxo-1,6-dihydropyridazine-3-carboxylic acid monohydrate (0.64 g, 3.6 mmol), chloroform (14 mL), dimethylformamide (0.1 mL) and thionyl chloride (1.2 mL) were added. The reaction mixture was stirred at 60° C. for 16 h. The reaction mixture was evaporated in vacuo to dryness. The solid residue was dissolved in dichloromethane (13 mL) and added dropwise to the mixture of cyclobutylethylamine (0.47 g, 4.74 mmol) and triethylamine (0.8 mL) in dichloromethane (25 mL) at ambient temperature. After stirred for 1 h, the reaction mixture was diluted with dichloromethane (100 mL) and washed sequentially with 10% aqueous HCl solution, saturated NaHCO3 and water. The organic layer was dried over Na2SO4 and evaporated in vacuum. Purification by column chromatography (silica gel, hexane/EtOAc (2:1)) afforded the product as a white powder (0.572 g, 59%). 1H NMR (300 MHz, CDCl3) δ 8.25, 7.97, 7.65, 3.42, 2.36, 2.08, 1.91-1.59.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759348B2
Source datasetuspto-grants-2010_07
ORD IDord-3db81e2f47cb41f7a8be485307023e81
Source noteuspto-grants-2010_07