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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29097생성일: 2026년 10월 24일

Triethylamine → Tert-butyl-[2-(5-phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-amine

https://huagongshe.com/ko/reaction/29097

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium CarbonateHCID 10340—
반응물PhenylacetyleneHCID 10821—
반응물[2-(5-Bromothiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-tert-butyl-amineHCID 69317100—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl-[2-(5-phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-amineHCID 1153085473.3%

반응 조건

온도50 °C

반응 단계

420 mg (1.2 mmol) of [2-(5-bromothiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-tert-butyl-amine were dissolved together with 0.33 ml (3.0 mmol) of phenylacetylene, 42 mg (0.06 mmol) of bis(triphenylphosphine)-palladium(II) chloride and 22 mg (0.12 mmol) of copper(I) iodide in DMF (9 ml). After addition of 1.6 ml (12.0 mmol) of triethylamine, the mixture was stirred at 50° C. for 16 h. The reaction solution was then diluted with EA and combined with a sat. aq. sodium carbonate solution. The phases were separated and the aqueous phase extracted with EA. The combined organic phases were washed 2× with a sat. aq. sodium carbonate solution and 2× with a sat. aq. common salt solution and dried over magnesium sulfate. After filtration and removal of the solvents under a vacuum, column chromatography (EA/DCM 1:4) was carried out with the group, after which 326 mg (0.88 mmol, 73% of theoretical) of tert-butyl-[2-(5-phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-amine were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420056B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-0708f3b4a08648e1a55002a67bb78689
출처 메모uspto-grants-2008_09