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HRID 55658作成日:2026年10月25日

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

https://huagongshe.com/reaction/55658

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Fumaric AcidHCID 444972—
反応物(R)-(-)-3-Bromo-2-methyl-1-propanolHCID 10441885—
反応物6-Fluoro-3-(4-piperidinyl)-1,2-benzisothiazoleHCID 18504976—
触媒Bis(tetrabutylammonium) sulphateHCID 11433187—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物(S)-6-Fluoro-3-[1-(3-hydroxy-2-methylpropyl)-4-piperidinyl]-1,2-benzisothiazole fumarateHCID 2286856969.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624927
出典データセットuspto-grants-1997_04
ORD IDord-6c01c24e89ac4d93a2d83773fd14c6d7
出典メモuspto-grants-1997_04