돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29102생성일: 2026년 10월 24일

2-Aminopyridine → [2-(5-Bromothiophen-2-yl)-imidazo[1,2-a]pyridin-3-yl]-(1,1,3,3-tetramethyl-butyl)-amine

https://huagongshe.com/ko/reaction/29102

반응식

참여 물질

역할이름HCID투입량
반응물2-AminopyridineHCID 10439—
반응물Perchloric AcidHCID 24247—
반응물1,1,3,3-Tetramethylbutyl isocyanideHCID 26725—
반응물5-Bromothiophene-2-carbaldehydeHCID 78428—
용매DichloromethaneHCID 6344—
생성물[2-(5-Bromothiophen-2-yl)-imidazo[1,2-a]pyridin-3-yl]-(1,1,3,3-tetramethyl-butyl)-amineHCID 6931791371%

반응 단계

235 mg (2.5 mmol) of 2-aminopyridine were dissolved together with 0.42 ml (2.5 mmol) of 1,1,3,3-tetramethyl-butylisonitrile and 0.27 ml (2.5 mmol) of 5-bromothiophene-2-carbaldehyde in DCM (5 ml). After addition of perchloric acid (0.25 ml), the mixture was stirred at RT for 5 d. Washing was then performed with a sat. aq. sodium carbonate solution and a sat. aq. common salt solution. The organic phase was dried over magnesium sulfate, filtered and evaporated under a vacuum. After carrying out column chromatography (EA/DIPE/DCM 2:2:1) with the group, 724 mg (1.7 mmol, 71% of theoretical) of [2-(5-bromothiophen-2-yl)-imidazo[1,2-a]pyridin-3-yl]-(1,1,3,3-tetramethyl-butyl)-amine were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420056B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-5240d8b45e85487baca690c674fe436e
출처 메모uspto-grants-2008_09