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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235628Generated: October 31, 2026

1-(4-Fluorophenyl)piperazine → 2-[3-[4-(4-fluorophenyl)-1-piperazinyl]propyl]-6,7-dimethyl-2H-1,4-benzothiazin-3(4H)-one

https://huagongshe.com/reaction/235628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
Reactant2-(3-bromopropyl)-6,7-dimethyl-2H-1,4-benzothiazin-3(4H)-oneHCID 13784613—
SolventEthyl AcetateHCID 8857—
Product2-[3-[4-(4-fluorophenyl)-1-piperazinyl]propyl]-6,7-dimethyl-2H-1,4-benzothiazin-3(4H)-oneHCID 1378464078.6%

Reaction Conditions

Temperature110 °C

Reaction Steps

In 10 ml of ethyl acetate were dissolved 628 mg of 2-(3-bromopropyl)-6,7-dimethyl-2H-1,4-benzothiazin-3(4H)-one and 721 mg of 1-(4-fluorophenyl)piperazine. The solution was concentrated and the concentrate was stirred at 110° C. for one hour, diluted with water, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over MgSO4 and concentrated to give 2-[3-[4-(4-fluorophenyl)-1-piperazinyl]propyl]-6,7-dimethyl-2H-1,4-benzothiazin-3(4H)-one (650 mg, 78.6%). Recrystallization from methanol gave colorless prisms, m.p. 161°-162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04640916
Source datasetuspto-grants-1987_02
ORD IDord-00d3682dc3a84113a1e9543fe0a112b5
Source noteuspto-grants-1987_02