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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424431Generated: November 2, 2026

Pentylamine → 6-Chloropyridazine-3-carboxylic acid pentylamide

https://huagongshe.com/reaction/2424431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentylamineHCID 8060—
ReactantThionyl ChlorideHCID 24386—
Reactant6-chloropyridazine-3-carboxylic AcidHCID 6415762—
Solvent1,4-DioxaneHCID 31275—
Product6-Chloropyridazine-3-carboxylic acid pentylamideHCID 4420315357.4%

Reaction Steps

To a flask containing 6-chloropyridazine-3-carboxylic acid (375 mg, 2.37 mmol) in dioxane (5 mL) was added thionyl chloride (420 mg, 0.26 mL, 3.56 mmol). The brown mixture was refluxed for 6 hours under nitrogen with stirring. After cooling to ambient temperature, the solvent was removed by rotary evaporator. The gummy black material was diluted with dioxane (5 mL) and the resulting solution was cooled in an ice-water bath. To the cooled solution was added amyl amine (410 mg, 0.55 mL, 4.74 mmol). The resulting black reaction solution was stirred at ambient temperature for 16 hours under nitrogen. The solvent was removed in vacuo and the residue was dissolved in dichloromethane (25 mL). The solution was washed with water (2×10 mL) and the organic layer was dried over MgSO4, filtered-off the solid and concentrated to afford a gummy material which was purified by column chromatography eluted with dichloromethane to yield 310 mg (57%) of the product as a colourless solid. m.p. 98-101° C. 1H NMR (300 MHz, CDCl3) δ 8.28, 8.05, 7.68, 3.51, 169-1.63, 0.90. MS (ES+) m/z 228 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964591B2
Source datasetuspto-grants-2011_06
ORD IDord-d77cb83f2d8048b2a6dbd0c47a890140
Source noteuspto-grants-2011_06