돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29107생성일: 2026년 10월 25일

Ethyl Acetate → N-tert-butyl-2-(5-(pyridin-2-ylethynyl)thiophen-2-yl)imidazo[1,2-a]pyridin-3-amine

https://huagongshe.com/reaction/29107

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Tert-Butyl isocyanideHCID 23577—
반응물AminopyrazineHCID 78747—
반응물5-Pyridin-2-ylethynyl-thiophene-2-carbaldehydeHCID 86230190—
촉매Scandium(III) triflateHCID 2734571—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물N-tert-butyl-2-(5-(pyridin-2-ylethynyl)thiophen-2-yl)imidazo[1,2-a]pyridin-3-amineHCID 1160317965%

반응 조건

온도80 °C

반응 단계

1.32 g (14.1 mmol) of 2-aminopyrazine were dissolved together with 3.00 g (14.1 mmol) of 5-pyridin-2-ylethynyl-thiophene-2-carbaldehyde, 1.59 ml (14.1 mmol) of tert.-butyl-isonitrile and 2.07 g (4.2 mmol) of scandium(III) trifluoromethanesulfonate in chloroform (40 ml). The reaction solution was heated to 80° C. for 60 min in the microwave (800 watt, MLS-Ethos1600) and then diluted with DCM. Washing was then performed with a 1M Na2CO3 solution and a sat. aq. NaCl solution. The mixture was then dried over Na2SO4, filtered and evaporated under a vacuum. 3.43 g (9.2 mmol, 65%) of N-tert-butyl-2-(5-(pyridin-2-ylethynyl)thiophen-2-yl)imidazo[1,2-a]pyridin-3-amine were obtained by crystallisation of the group from EA.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420056B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-a86679d007254961b57e7e2291097dfc
출처 메모uspto-grants-2008_09