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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2381053생성일: 2026년 10월 27일

Propylphosphonic anhydride → 2-[2-(Aminocarbonylmethoxy)-6-methoxyphenyl]-3-(2,6-dimethylphenylamino)-6-fluoroimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/2381053

반응식

참여 물질

역할이름HCID투입량
반응물Propylphosphonic anhydrideHCID 111923—
반응물N-(2,6-Dimethylphenyl)formamideHCID 345859—
반응물2-Amino-5-fluoropyridineHCID 2737701—
반응물Propylphosphoric anhydrideHCID 16167369—
반응물2-(2-Formyl-3-methoxyphenoxy)acetamideHCID 42604614—
용매TriethylamineHCID 8471—
생성물2-[2-(Aminocarbonylmethoxy)-6-methoxyphenyl]-3-(2,6-dimethylphenylamino)-6-fluoroimidazo[1,2-a]pyridineHCID 24854988—

반응 조건

온도100 °C

반응 단계

4.2 0.149 g of 12, 0.112 g of 2-amino-5-fluoropyridine 4, 0.209 g of 2-(2-formyl-3-methoxyphenoxy)acetamide 3, 0.286 ml of triethylamine and, dropwise, 2.5 ml of T3P® [=propylphosphonic anhydride (50% solution in ethyl acetate)] are introduced successively into a flask with ice-cooling and under an inert gas. The reaction mixture is stirred at 100° C. for 7 h. The mixture is subsequently subjected to conventional work-up, giving 0.2 g (40%) of “A1”.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08258151B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-df4dd51a7ae14f998fd7e0c33560e0bc
출처 메모uspto-grants-2012_09