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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437300Generated: November 2, 2026

Acetyl chloride → HCID 23090451, compound

https://huagongshe.com/reaction/1437300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 23090518HCID 23090518—
SolventDichloromethaneHCID 6344—
ProductHCID 23090451HCID 23090451—

Reaction Steps

At 0° C., triethylamine (0.205 mL) and acetyl chloride (0.0447 mL) were added to a solution of 4-[1-(6-methoxy-3-pyridyl)-5-(2-pyridyl)pyrazole-3-carbonyl]piperazine hydrochloride (0.185 g) obtained in Example 81 in methylene chloride (5.0 mL). The mixture was stirred at room temperature for 1 hour. The reaction mixture was partitioned between water and chloroform. The aqueous layer was further extracted with chloroform, and the organic layers were combined, followed by washing with saturated brine and drying over sodium sulfate anhydrate. After filtration, the solvent was removed under reduced pressure. The residue was purified through silica gel column chromatography (chloroform-methanol), to thereby give the title compound as an amorphous product (0.147 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622471B2
Source datasetuspto-grants-2009_11
ORD IDord-b7abd60efde64bef83ae946b99076ecb
Source noteuspto-grants-2009_11