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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059276Generated: November 1, 2026

Pyridine → 10-methoxymethyl-8-chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazine

https://huagongshe.com/reaction/1059276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant10-Methoxymethyl-10H-pyrazino[2,3-b][1,4]benzothiazine-8-methanolHCID 11265817—
ReactantSodium bicarbonate methylene chlorideHCID 23716255—
SolventDimethylformamideHCID 6228—
Product10-methoxymethyl-8-chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazineHCID 11335363—

Reaction Steps

Into a solution of 19 g of 10-methoxymethyl-10H-pyrazino[2,3-b][1,4]benzothiazine-8-methanol and 13.9 ml of pyridine in N,N-dimethylformamide (150 ml) was added dropwise under a nitrogen atmosphere 13.3 ml of methanesulfonyl chloride at 0° C. Then the reaction mixture was stirred at room temperature for 1 hour and then poured into a pre-cooled aqueous solution of methylene chloride/sodium hydrogen carbonate. Then it was extracted with ethyl acetate, washed with water and dried over anhydrous sodium sulfate. After distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (eluted with methylene chloride) to thereby give 13.6 g of the title compound as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518423B1
Source datasetuspto-grants-2003_02
ORD IDord-6e0c648fc1ad4023939b914dad7b3e89
Source noteuspto-grants-2003_02