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HRID 652136作成日:2026年10月25日

Phenethyl bromide → 1-(2-Phenylethyl)-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromide

https://huagongshe.com/reaction/652136

反応式

関与物質

役割名称HCID仕込み量
反応物Phenethyl bromideHCID 7666—
反応物Sodium hydrideHCID 24758—
反応物Ether hydrobromideHCID 86739792—
反応物HCID 178480237HCID 178480237—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物1-(2-Phenylethyl)-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromideHCID 1403251136%

反応手順

To a stirred mixture of 0.86 g of sodium hydride (50% oil dispersion) in 50 ml of dimethylformamide was added, dropwise, 3.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole in 15 ml of hot dimethylformamide. The reaction mixture was stirred at ambient temperature for 1 hr and then a solution of 3.33 g of (2-bromoethyl)benzene in 10 ml of dimethylformamide was added dropwise. The reaction mixture was stirred for 21/2 days at ambient temperature, cooled to 0°, and water was added dropwise. The mixture was extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield an oil. The oil was dissolved in ether and a saturated hydrogen bromide/ether solution was added dropwise. The resultant solid was recrystallized two times from ethanol to yield 2.0 g (36%) of product, mp 163°-164° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04670447
出典データセットuspto-grants-1987_06
ORD IDord-21f347a238924514af23d85af2ba5572
出典メモuspto-grants-1987_06