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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55658생성일: 2026년 10월 24일

Potassium Carbonate → (S)-6-Fluoro-3-[1-(3-hydroxy-2-methylpropyl)-4-piperidinyl]-1,2-benzisothiazole fumarate

https://huagongshe.com/ko/reaction/55658

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Fumaric AcidHCID 444972—
반응물(R)-(-)-3-Bromo-2-methyl-1-propanolHCID 10441885—
반응물6-Fluoro-3-(4-piperidinyl)-1,2-benzisothiazoleHCID 18504976—
촉매Bis(tetrabutylammonium) sulphateHCID 11433187—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물(S)-6-Fluoro-3-[1-(3-hydroxy-2-methylpropyl)-4-piperidinyl]-1,2-benzisothiazole fumarateHCID 2286856969.1%

반응 단계

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisothiazole (4.6 g, 20 mmol), (R)-(-)-3-bromo-2-methyl-1-propanol (3.0 g, 20 mmol), K2CO3 (2.7 g, 20 mmol), tetrabutylammonium sulfate (0.058 g), CH3CN (95 ml) and H2O (19 ml) was stirred and refluxed for 4.5 hours. After standing at ambient temperature for 16 hours, the reaction was poured into H2O, and subsequent extractive workup of the aqueous with EtOAc yielded 6.8 g of a partially solidified oil. The product was purified by flash chromatography on silica gel, eluting the column with CH2Cl2, then 2% MeOH--CH2Cl2 and finally 5% MeOH--CH2Cl2. Concentration of the appropriate fractions yielded 5.2 g of a waxy solid. The solid was dissolved in acetone and fumaric acid (1.9 g, 1.0 eq) was added and the reaction briefly heated at reflux. The resultant fumarate salt precipitated from solution yielding 4.8 g of white solid. The compound was recrystallized from acetonitrile to yield 3.1 g (36%) of the alcohol as a white solid, m.p.=151°-153° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624927
출처 데이터셋uspto-grants-1997_04
ORD IDord-6c01c24e89ac4d93a2d83773fd14c6d7
출처 메모uspto-grants-1997_04