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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1813899Generated: October 30, 2026

Pyridine → HCID 10090742, compound

https://huagongshe.com/reaction/1813899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 10286610HCID 10286610—
SolventDichloromethaneHCID 6344—
ProductHCID 10090742HCID 10090742—

Reaction Steps

3-Benzenesulfonyl-2-methylsulfanyl-pyrido[1,2-a]pyrimidin-4-ylideneamine (100 mg, 0.30 mmol) was dissolved in anhydrous methylenechloride (2 ml) to which pyridine (48 mg, 0.6 mmol) was added. Acetylchloride was then added at room temperature and the reaction mixture was stirred overnight. The reaction was quenched with saturated aqueous NaHCO3, extracted with methylene chloride, and purified by flash chromatography to yield 79 mg of a yellow solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875771B2
Source datasetuspto-grants-2005_04
ORD IDord-4d002db4e2714d608e85f2dd2a17b015
Source noteuspto-grants-2005_04