Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235634Generated: October 31, 2026

1-(4-Fluorophenyl)piperazine → HCID 13784684, compound

https://huagongshe.com/reaction/235634

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
ReactantHCID 13784632HCID 13784632—
SolventEthyl AcetateHCID 8857—
ProductHCID 13784684HCID 13784684—

Reaction Conditions

Temperature110 °C

Reaction Steps

In 10 ml of ethyl acetate were dissolved 435 mg of 2-(4-chlorobutyl)-2H-1,4-benzothiazin-3(4H)-one and 613 mg of 1-(4-fluorophenyl)piperazine. The solvent was evaporated off, and the residue was stirred at 110° C. for one hour. The reaction mixture was extracted with ethyl acetate, and the extract was washed with water and dried (MgSO4). After removal of the solvent, the residue was subjected to a column chromatography on silica-gel (40 g). From the eluate with hexane-ethyl acetate (1:1, v/v) was obtained 2-[4-[4-(4-fluorophenyl)-1-piperazinyl]butyl]-2H-1,4-benzothiazin-3(4H)-one. The yield was 293 mg (43.2%). Recrystallization from methanol gave prisms, m.p. 150°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04640916
Source datasetuspto-grants-1987_02
ORD IDord-a14e84e5bd084f6cbf3fecf79c2cbbdc
Source noteuspto-grants-1987_02