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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059278Generated: November 3, 2026

Trifluoroacetic acid → 8-Chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazine

https://huagongshe.com/reaction/1059278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
Reactant10-methoxymethyl-8-chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazineHCID 11335363—
SolventDichloromethaneHCID 6344—
Product8-Chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazineHCID 1174703883.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into 250 ml of a solution of 26.9 g of 8-chloromethyl-10-methoxymethyl-10H-pyrazino[2,3-b][1,4]benzothiazine in methylene chloride was dropped 50 ml of trifluoroacetic acid at 0° C. After reacting at room temperature for 12 hours, the reaction mixture was cooled to 0° C. and neutralized by adding an aqueous solution of sodium hydrogencarbonate. The crystals thus precipitated were taken up by filtration and washed successively with water and diethyl ether to thereby give 19.1 g of the title compound as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518423B1
Source datasetuspto-grants-2003_02
ORD IDord-a4fe67fb396c4809b613d57a387c8948
Source noteuspto-grants-2003_02