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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233222생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/233222

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물Ethyl 3-bromopropionateHCID 68320—
반응물6-Fluoro-3-(4-piperidinyl)-1,2-benzisothiazoleHCID 18504976—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 3-[4-(6-Fluoro-1,2-benzisothiazol-3-yl)-1-piperidinyl]propionate hydrochlorideHCID 1846724864%

반응 단계

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 was 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591745
출처 데이터셋uspto-grants-1997_01
ORD IDord-22b4f63b84cf4cff9079a0e5ea2a035d
출처 메모uspto-grants-1997_01