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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14생성일: 2026년 10월 23일

4-Amino-3-methoxybenzaldehyde → 4-(5-Chloro-4-(imidazo[1,2-a]pyridin-3-yl)pyrimidin-2-ylamino)-3-methoxybenzaldehyde

https://huagongshe.com/ko/reaction/14

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참여 물질

역할이름HCID투입량
반응물4-Amino-3-methoxybenzaldehydeHCID 19765052—
반응물3-(2,5-Dichloropyrimidin-4-yl)imidazo[1,2-a]pyridineHCID 46934605—
시약1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물4-(5-Chloro-4-(imidazo[1,2-a]pyridin-3-yl)pyrimidin-2-ylamino)-3-methoxybenzaldehydeHCID 5929105234.9%

반응 조건

온도120 °C

반응 단계

3-(2,5-dichloropyrimidin-4-yl)imidazo[1,2-a]pyridine (4 g, 15.09 mmol), 4-amino-3-methoxybenzaldehyde (2.281 g, 15.09 mmol), 9,9-DIMETHYL-4,5-BIS(DIPHENYLPHOSPHINO)XANTHENE (0.873 g, 1.51 mmol), TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM (0.345 g, 0.38 mmol) and 1,8-DIAZABICYCLO [5.4.0] UNDEC-7-ENE (5.64 ml, 37.72 mmol) were dissolved in Dioxane (120 ml) then degazed and purged with argon. The reaction was heated to reflux (bath 120°C) for 2H30. Reaction mixture was filtered through a filter cup and concentrated. FR01132-77-01 w=14.65 g The crude product was purified by flash chromatography (NOVASEP) on silica gel ( 15-40µm ) eluting with 0 to 5% methanol in dichloromethane. The solvent was evaporated to dryness to afford 4-(5-chloro-4-(imidazo[1,2-a]pyridin-3-yl)pyrimidin-2-ylamino)-3-methoxybenzaldehyde (34.9 %) as a clear yellow solid. PBO-01132-77-02 w=2 g

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-4695ad3979554c448a445867cc030440
출처 메모750 AstraZeneca ELN dataset