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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423423Generated: November 3, 2026

Pyridine → HCID 66674274, compound

https://huagongshe.com/reaction/423423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 66674020HCID 66674020—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 66674274HCID 6667427490.2%

Reaction Steps

Add pyridine (0.50 mL, 6.18 mmol) to a mixture of 2-(4-chloro-phenyl)-6-[6-(piperidin-4-yloxy)-pyridin-3-yl]-6H-thieno[2,3-c]pyridin-7-one, hydrochloride (0.741 g, 1.56 mmol) in dichloromethane at room temperature. After stirring for 5 min, add acetyl chloride (0.16 mL, 2.33 mmol) to the mixture and stir overnight at room temperature. Dilute the mixture with water, extract into dichloromethane (3×50 mL), then dry over sodium sulfate, filter, and concentrate. Purify the residue using silica gel flash column chromatography (1-3% methanol/dichloromethane) and concentrate on high vacuum to yield the titled compound (0.678 g, 90%). MS/ES m/z (37Cl) 483 [M+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101764B2
Source datasetuspto-grants-2012_01
ORD IDord-03f5b0b4190f43a5993364a1e17f7848
Source noteuspto-grants-2012_01