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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068917Generated: October 30, 2026

Phosphorus oxychloride → 4-Chloro-1,5-dimethyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acid

https://huagongshe.com/reaction/2068917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant4-Hydroxy-1,5-dimethyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acidHCID 57442168—
CatalystDimethylformamideHCID 6228—
Product4-Chloro-1,5-dimethyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acidHCID 6667325730.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-hydroxy-1,5-dimethyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acid (35.4 g, 192 mmol), catalytic amount of DMF (3 drop), and POCl3 (178 mL, 1.92 mol) was heated for 2 days at 90° C., and then the POCl3 was removed under reduced pressure. The crude material was quenched with ice, and the reaction mixture was stirred for 2 hours at room temperature. The precipitates formed out of the solution was filtered off and washed with ether. The precipitates collected were triturated with ether to afford 11.7 g (30%) of the desired product. The filtrate was extracted with EtOAc (2×). The combined organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure to give the crude product that was triturated with ether and dried under reduced pressure to afford additional 9.56 g (24%) of the desired product. A total of 21.29 g (55%) of the desired product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299076B2
Source datasetuspto-grants-2012_10
ORD IDord-f66f5534b8ab435abf13be61cf64ccca
Source noteuspto-grants-2012_10