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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ethyl Bromide | HCID 6332 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Dichloromethane ethylacetate | HCID 21226138 | — |
| 반응물 | 2-(5-Phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-ylamine hydrochloride | HCID 69319360 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Ethyl-[2-(5-phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-amine | HCID 11573751 | 92.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07420056B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-bce83af9c2454030b10934d6475f3838 |
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| 출처 메모 | uspto-grants-2008_09 |
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