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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 427485생성일: 2026년 10월 25일

Methylamine → 8-(2-ethyl-6-methylbenzylamino)-N, 2,3-trimethylimidazo[1,2-a]pyridine-6-carboxamide

https://huagongshe.com/reaction/427485

반응식

참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물2,3-Dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo[1,2-a]pyridine-6-carboxylic acidHCID 11823936—
용매DichloromethaneHCID 6344—
생성물8-(2-ethyl-6-methylbenzylamino)-N, 2,3-trimethylimidazo[1,2-a]pyridine-6-carboxamideHCID 986324226%

반응 단계

2,3-Dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo[1,2-a]pyridine-6-carboxylic acid (0.15 g, 0.44 mmol) and o-Benzotriazol-1-yl-N,N,N′,N′-Tetramethyluronium tetrafluoroborate (TBTU) (0.14 g, 0.44 mmol) were added to methylene chloride (10 ml) and the reaction mixture was stirred at room temperature for 15 min. Methylamine (0.1 g, 3.2 mmol) was added and the reaction mixture was stirred at ambient temperature for 1.5 h. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography on silica gel using ethylacetate:methylene chloride (1:1) as eluent. The yield was treated with diethyl ether to give 40 mg (26%) of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313137B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-21e4605fc6fd4ff89efa148354f82356
출처 메모uspto-grants-2001_11