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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111112Generated: November 2, 2026

Hydrochloric Acid → Methyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylate

https://huagongshe.com/reaction/2111112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant4-Chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acidHCID 66674132—
SolventMethanolHCID 887—
ProductMethyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylateHCID 5788621117%

Reaction Steps

A solution of 4-chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acid (390 mg, 2.07 mmol) and conc. HCl (0.10 mL) in MeOH (6 mL) was refluxed for 8 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure to give the crude material that was redissolved into EtOAc. The organic layer was washed with water, dried over MgSO4, filtered, and concentrated under reduced pressure to give the crude material that was purified by silica gel flash column chromatography (100% hexanes to 10 to 20 to 30 to 50% EtOAc in hexanes) to afford 72 mg (17%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517994B2
Source datasetuspto-grants-2009_04
ORD IDord-05bbeb696ec7405e8ab07c8cfd33d437
Source noteuspto-grants-2009_04