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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706057Generated: October 25, 2026

Thionyl Chloride → HCID 178480221, compound

https://huagongshe.com/reaction/706057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium borohydrideHCID 4311764—
Reactant5-[(1-methyl-1H-pyrazol-4-yl)methyl]-2-thioxo-2,3-dihydro-4(1H)-pyrimidinoneHCID 21936385—
Reactant4-[(4-Chloro-2-pyridinyl)oxy]benzaldehydeHCID 23433214—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 178480221HCID 17848022158.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-[(4-chloro-2-pyridinyl)oxy]benzaldehyde (120 mg, 0.514 mmol), (which may be prepared according to procedures described in the International Patent Application Publication No. WO 199847869) in methanol (2.0 mL) was added NaBH4 (23.32 mg, 0.616 mmol). After the suspended solution turned clear, it was quenched with water. The mixture was extracted with EA and concentrated. After removing the solvent, thionyl chloride (0.187 mL, 2.57 mmol) and DCM (2 mL) was added, and stirring continued overnight. Then 5-[(1-methyl-1H-pyrazol-4-yl)methyl]-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone (114 mg, 0.514 mmol) was added. The reaction mixture was heated at 60° C. for 0.5 h. Purification via MDAP then afforded the title compound (132 mg, 58.4% yield). LCMS: rt=2.84 min, [M+H+]=440

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-adc99a90465643dbab966f2feb989356
Source noteuspto-grants-2015_11