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HRID 434406作成日:2026年10月27日

Ammonium Chloride → 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-hydroxy-4-(4-methoxyphenyl)piperidine hydrochloride

https://huagongshe.com/reaction/434406

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-piperidoneHCID 13207819—
反応物HCID 178418276HCID 178418276—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-hydroxy-4-(4-methoxyphenyl)piperidine hydrochlorideHCID 13207827—

反応手順

A solution of 6.3 g of 1-[3-(6-fluoro-1,2-benzisoxazol-3-yl)propyl]-4-piperidone in 35 ml of tetrahydrofuran was slowly added to a solution of 49 ml of p-anisylmagnesium bromide (1.4 M in tetrahydrofuran). After the addition was complete, the reaction mixture was stirred at ambient temperature for one hr, diluted with ether, poured into 400 of ml saturated ammonium chloride solution and extracted with ether. The organic extracts were washed with water (2×), saturated sodium chloride solution and dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was converted to 8.5 g (89%) of product, mp 100°-105° C., by treatment with ethereal hydrogen chloride. An analytical sample was obtained by recrystallization from ethyl acetate/methanol and had mp 181°-182° C. (dec).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04396770
出典データセットuspto-grants-1983_08
ORD IDord-c19ce0116b8849bba4849a32a844be42
出典メモuspto-grants-1983_08