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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184567Generated: October 31, 2026

Hydrochloric Acid → Ethyl 3-[4-(6-Fluoro-1,2-benzisothiazol-3-yl)-1-piperidinyl]propionate hydrochloride

https://huagongshe.com/reaction/2184567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Fluoro-3-(4-piperidinyl)-1,2-benzisothiazoleHCID 18504976—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-[4-(6-Fluoro-1,2-benzisothiazol-3-yl)-1-piperidinyl]propionate hydrochlorideHCID 1846724864%

Reaction Steps

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisothiazole (6.0 g, 25 mmol) ethyl 3-bromopropionate (4.5 g, 25 mmol), K2CO3 (3.5 g) and CH3CN (100 ml) was stirred and refluxed for 16 hours. The reaction was poured into H2O, and after extractive workup with EtOAc, 6.0 g of an orange oil was realized. The oil was dissolved in Et2O and ethereal HCl and added to precipitate 6.3 g of a white hydrochloride salt. The salt was recrystallized from CH3CN to yield 6.0 g (64% ) of the desired compound. An analytical sample was obtained by recrystallization of a 1.0 g sample from EtOH-Et2O to yield 0.8 g of a white solid, m.p.=197°-199° C. ANALYSIS: Calculated for C17H21FN2O2S.HCl: 54.76% C 5.95% H 7.51% N Found: 54.77% C 5.99% H 7.28% N

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037729E1
Source datasetuspto-grants-2002_06
ORD IDord-bc9631e639d149d99488b3958728a8de
Source noteuspto-grants-2002_06