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HRID 55645作成日:2026年10月25日

Potassium Carbonate → 1-(3-Dimethylaminopropyl)-4-(6-fluoro-1,2-benzisoxazol-yl)piperidine difumarate

https://huagongshe.com/reaction/55645

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3-(Dimethylamino)propyl chloride hydrochlorideHCID 94308—
反応物Fumaric AcidHCID 444972—
反応物3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
触媒Tetrabutylammonium hydrogen sulfateHCID 94433—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物1-(3-Dimethylaminopropyl)-4-(6-fluoro-1,2-benzisoxazol-yl)piperidine difumarateHCID 6707110056.9%

反応条件

温度60 °C

反応手順

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (3.05 g, 13.8 mmol), 3-dimethylaminopropyl chloride hydrochloride (3.4 g, 21 mmol), K2CO3 (6.2 g, 45 mmol), tetrabutylammonium hydrogen sulfate (phase transfer catalyst, 1.5 g) in acetonitrile (100 ml) and water (50 ml) was heated at 60° C. overnight. The aqueous phase was separated, and acetonitrile was removed at reduced pressure. The residue was extracted into DCM. The organic solution was washed with H2O and brine, then dried with MgSO4. The solvent was removed and the crude product (4.3 g) was treated with fumaric acid (1.58 g, 1.0 eq) in dilute ethanol. The crystals were collected (2.53 g), m.p.=192°-194° C. Recrystallization from ethanol yielded 2.08 g of white crystals, mp=194°-195° 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-abf3cdd92c534119b808c05d65a1a1c9
出典メモuspto-grants-1997_04