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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357418생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/357418

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
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—
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), K2 CO3 (2.7 g, 20 mmol), tetrabutylammonium sulfate (0.058 g), CH3 CN (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 번호US05840727
출처 데이터셋uspto-grants-1998_11
ORD IDord-3fc8b1e9080447b2b4041f5cf01c12a3
출처 메모uspto-grants-1998_11