돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29106생성일: 2026년 10월 25일

Ethyl Bromide → Ethyl-[2-(5-phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-amine

https://huagongshe.com/reaction/29106

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl BromideHCID 6332—
반응물Sodium hydrideHCID 24758—
반응물Dichloromethane ethylacetateHCID 21226138—
반응물2-(5-Phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-ylamine hydrochlorideHCID 69319360—
용매DimethylformamideHCID 6228—
생성물Ethyl-[2-(5-phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-amineHCID 1157375192.5%

반응 단계

395 mg (1.25 mmol) of 2-(5-phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-ylamine hydrochloride (Example 83) were dissolved in DMF (8 ml). After addition of 100 mg (2.5 mmol) of sodium hydride (60% dispersion in mineral oil), the mixture was stirred at RT for 1 h. A solution of 74 μl (0.8 mmol) of ethyl bromide in DMF (2 ml) was then added dropwise. The reaction solution was stirred at RT for 16 h, quenched with water (10 ml) and extracted with EA (2×50 ml). The combined organic phases were dried over MgSO4, filtered and evaporated under a vacuum. 253 mg (0.74 mmol, 58% of theoretical) of ethyl-[2-(5-phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-amine were obtained by means of column chromatography (silica gel, EA/DCM 4:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420056B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-bce83af9c2454030b10934d6475f3838
출처 메모uspto-grants-2008_09