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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235631Generated: November 1, 2026

Sodium Iodide → HCID 13784678, compound

https://huagongshe.com/reaction/235631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
Reactant2-(2-chloroethyl)-4-methyl-2H-1,4-benzothiazin-3(4H)-oneHCID 20220106—
SolventDimethylformamideHCID 6228—
ProductHCID 13784678HCID 13784678—

Reaction Conditions

Temperature100 °C

Reaction Steps

To 15 ml of dimethylformamide were added 1.21 g of 2-(2-chloroethyl)-4-methyl-2H-1,4-benzothiazin-3(4H)-one, 1.08 g of 1-(4-fluorophenyl)piperazine, 0.69 g of potassium carbonate and 0.05 g of sodium iodide. The mixture was stirred at 100° C. for 4 hours. The reaction solution was poured into ice-water and extracted with dichloromethane. The dichloromethane layer was washed with water and dried (MgSO4). Then, the solvent was evaporated off. The residue was subjected to a column chromatography on silica-gel (130 g). From the eluate with hexane-ethyl acetate (1:1, v/v) was obtained 2-[2-[4(4-fluorophenyl)-1-piperazinyl]ethyl]-4-methyl-2H-1,4-benzothiazin-3(4H)-one as an oily substance. This product was treated with methanol saturated with hydrogen chloride to give crystals of its hydrochloride. The yield was 0.99 g (43.2%). Recrystallization from methanol-ether gave prisms, m.p. 202°-204° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04640916
Source datasetuspto-grants-1987_02
ORD IDord-42f751079ace4096bd322dfef973425a
Source noteuspto-grants-1987_02