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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059421Generated: October 30, 2026

Dichloromethane → HCID 23564544, compound

https://huagongshe.com/reaction/1059421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantThionyl ChlorideHCID 24386—
Reactant[N-(2-Pyridyl)aminometyl](10-methoxymethyl-10H-pyrazino[2,3-b][1,4]benzothiazin-8-yl)ketoneHCID 23565187—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 23564544HCID 2356454461.6%

Reaction Steps

10 ml of a solution of 200 mg of [N-(2-pyridyl)aminometyl](10-methoxymethyl-10H-pyrazino[2,3-b][1,4]benzothiazin-8-yl)ketone in carbon tetrachloride was stirred at room temperature and 240 mg of thionyl chloride was dropped thereinto. The reaction mixture was distributed into dichloromethane and an aqueous solution of sodium bicarbonate and the organic layer was separated. To the organic layer were added methanol and tetrahydrofuran to give a homogeneous solution. After adding silica gel and distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (eluted with dichloromethane/methanol) to thereby give 103 mg of the title compound as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518423B1
Source datasetuspto-grants-2003_02
ORD IDord-ce1339966b1f4c70899cfbbe10757b5f
Source noteuspto-grants-2003_02