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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 845613생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/845613

반응식

참여 물질

역할이름HCID투입량
반응물Phenethyl bromideHCID 7666—
반응물Sodium hydrideHCID 24758—
반응물Ether hydrobromideHCID 86739792—
반응물HCID 178480237HCID 178480237—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물1-(2-Phenylethyl)-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromideHCID 1403251136%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04758668
출처 데이터셋uspto-grants-1988_07
ORD IDord-401631fb0d944a8c9ea03ef704fc20da
출처 메모uspto-grants-1988_07