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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 427520생성일: 2026년 10월 25일

Triethylamine → 2,3-Dimethyl-8-(2-(2-(benzyloxy)ethyl)-6-methylbenzylamino)-imidazo[1,2-a]pyridine-6-carboxamide

https://huagongshe.com/reaction/427520

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물8-Amino-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxamide mesylateHCID 18357435—
반응물2-[2-(Benzyloxy)ethyl]-6-methylbenzaldehydeHCID 18357452—
촉매ZincchlorideHCID 3007855—
용매MethanolHCID 887—
생성물2,3-Dimethyl-8-(2-(2-(benzyloxy)ethyl)-6-methylbenzylamino)-imidazo[1,2-a]pyridine-6-carboxamideHCID 121489207.7%

반응 단계

To a solution of 8-Amino-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxamide mesylate 1.4 g (0.0038 mol) in methanol (20 ml) in a nitrogen atmosphere was added zinc chloride (1.0 g, 0.0039 mol) solved in methanol(10 ml) and the mixture was stirred for 30 min. To the mixture were added 2-[2-(benzyloxy)ethyl]-6-methylbenzaldehyde (1.0 g, 0.0039 mol) and sodium cyano borohydride (0.48 g, 0.0076 mol) and the mixture was refluxed overnight. The reation mixture was cooled to room temperature, triethylamine (4 ml) was added, the mixture was stirred for 30 min, and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using methylene chloride:methanol (9:1) as eluent. The residue was solved in diethyl ether, treated with diethyl ether/HCl and the precipitated product as HCl salt was filtered off . The salt was soloved in methylene chloride and washed with saturated sodium carbonate. The organic layer was separated, washed with water, dried and evaporated under reduced pressure to give 0.13 g (7.7 g) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313137B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-f53561ec9cae492e8b261122fc119cf6
출처 메모uspto-grants-2001_11