Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235630Generated: October 26, 2026

1-(4-Fluorophenyl)piperazine → 2-[2-[4-(4-fluorophenyl)-1-pyrazinyl]ethyl]-2H-1,4-benzothiazin-3(4H)-one

https://huagongshe.com/reaction/235630

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
Reactant2-(2-bromoethyl)-3,4-dihydro-2H-1,4-benzothiazin-3-oneHCID 13784623—
SolventEthyl AcetateHCID 8857—
Product2-[2-[4-(4-fluorophenyl)-1-pyrazinyl]ethyl]-2H-1,4-benzothiazin-3(4H)-oneHCID 20220108—

Reaction Conditions

Temperature110 °C

Reaction Steps

In 20 ml of ethyl acetate were dissolved 1.36 g of 2-(2-bromoethyl)-2H-1,4-benzothiazin-3(4H)-one and 1.8 g of 1-(4-fluorophenyl)piperazine. The solvent was evaporated off, and the residue was stirred at 110° C. for one hour. The reaction product was extracted with ethyl acetate, and the extract was washed with water and dried over MgSO4. The crystals obtained by evaporation of the solvent were recrystallized from methanol to give 2-[2-[4-(4-fluorophenyl)-1-pyrazinyl]ethyl]-2H-1,4-benzothiazin-3(4H)-one as prisms, m.p. 158°-159° C. The yield was 0.94 g (50.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04640916
Source datasetuspto-grants-1987_02
ORD IDord-8c226101b90a48d6a2efd64baa8aca18
Source noteuspto-grants-1987_02