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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4300생성일: 2026년 10월 24일

2-Amino-3-benzyloxypyridine → 8-Benzyloxy-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridine

https://huagongshe.com/ko/reaction/4300

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-3-benzyloxypyridineHCID 90334—
반응물3-Tosyloxy-5-hexyn-2-oneHCID 13825893—
용매EthanolHCID 702—
생성물8-Benzyloxy-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridineHCID 1382589731%

반응 단계

A solution of 2-amino-3-benzyloxypyridine (2 g) and 3-tosyloxy-5-hexyn-2-one (2.66 g) in ethanol (15 ml) was stirred and refluxed for 24 hours and then evaporated in vacuo. To the residue was added an aqueous solution of sodium bicarbonate and the mixture was extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and evaporated in vacuo. The oily residue was purified by column chromatography on silica gel (50 g) using chloroform as an eluent to give a solid, which was recrystallized from a mixture of methylene chloride and diethyl ether to give 8-benzyloxy-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridine (0.855 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04725601
출처 데이터셋uspto-grants-1988_02
ORD IDord-30e0a8c847e3408db73ba26ed7bed814
출처 메모uspto-grants-1988_02