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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 161생성일: 2026년 10월 23일

Tert-butyl 2-((4-amino-3-methoxyphenyl)(methyl)amino)acetate → Tert-butyl 2-((4-(5-chloro-4-(8-fluoroimidazo[1,2-a]pyridin-3-yl)pyrimidin-2-ylamino)-3-methoxyphenyl)(methyl)amino)acetate

https://huagongshe.com/ko/reaction/161

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참여 물질

역할이름HCID투입량
반응물Tert-butyl 2-((4-amino-3-methoxyphenyl)(methyl)amino)acetateHCID 68592384—
반응물3-(2,5-Dichloropyrimidin-4-yl)-8-fluoroimidazo[1,2-a]pyridineHCID 86641172—
시약Potassium Phosphate, TribasicHCID 62657—
촉매Binap, (A+-)-HCID 634876—
촉매Palladium (II) acetateHCID 4144353—
용매1,4-DioxaneHCID 31275—
생성물Tert-butyl 2-((4-(5-chloro-4-(8-fluoroimidazo[1,2-a]pyridin-3-yl)pyrimidin-2-ylamino)-3-methoxyphenyl)(methyl)amino)acetateHCID 6859079343.05%

반응 조건

온도100 °C

반응 단계

A microwave tube was charged with diacetoxypalladium (11.18 mg, 0.05 mmol), potassium phosphate (529 mg, 2.49 mmol),2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (62.0 mg, 0.10 mmol), 3-(2,5-dichloropyrimidin-4-yl)-8-fluoroimidazo[1,2-a]pyridine (282 mg, 1.00 mmol) purged with nitrogen. Dioxane (4.5 ml) was added followed by tert-butyl 2-((4-amino-3-methoxyphenyl)(methyl)amino)acetate (292 mg, 1.10 mmol). The resulting suspension was purged again and was heated at 100 °C for 1h30. After cooling, the mixture was filtered through a pad of Dicalite speed plus and washed with dichloromethane. The solvent were evaporated. PBO-01970-51-01 The crude product was purified by flash chromatography on silica gel (Merck cartridge SVF D26 - SI60 15-40µm - 30g) eluting with 0 up to 50% EtOAc in petroleum ether. Collected fractions were evaporated to afford tert-butyl 2-((4-(5-chloro-4-(8-fluoroimidazo[1,2-a]pyridin-3-yl)pyrimidin-2-ylamino)-3-methoxyphenyl)(methyl)amino)acetate (220 mg, 43.1 %) as a clear yellow solid. PBO-01970-51-02

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-e759d69f11ae4651a16a93e70cd9c7e3
출처 메모750 AstraZeneca ELN dataset