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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211889Generated: October 31, 2026

2-Fluorobenzenesulphonyl chloride → HCID 21963248, compound

https://huagongshe.com/reaction/2211889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorobenzenesulphonyl chlorideHCID 137761—
ReactantHCID 21963416HCID 21963416—
ProductHCID 21963248HCID 21963248—

Reaction Steps

N-{2-[3-(4-1,2-Benzisothiazol-3-yl-piperazin-1-yl)-propyl]-phenyl}-2-fluoro-benzenesulfonamide was prepared according to the procedure outlined in Example 44, starting with 2-[3-(4-1,2-benzisothiazol-3-yl-piperazin-1-yl)-propyl]-phenylamine (150 mg) and 2-fluorobenzenesulfonyl chloride (55 mg). The resultant white solid was purified using an ISCO autocolumn eluting with 100% ethyl acetate. N-{2-[3-(4-1,2-Benzisothiazol-3-yl-piperazin-1-yl)-propyl]-phenyl}-2-fluoro-benzenesulfonamide was isolated in 100% purity @ 254 nm; LCMS (APCI): 511 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101886B2
Source datasetuspto-grants-2006_09
ORD IDord-de7958d010754a17a48c589e7933e28a
Source noteuspto-grants-2006_09