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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Propylphosphonic anhydride | HCID 111923 | — |
| 반응물 | N-(2,6-Dimethylphenyl)formamide | HCID 345859 | — |
| 반응물 | 2-Amino-5-fluoropyridine | HCID 2737701 | — |
| 반응물 | Propylphosphoric anhydride | HCID 16167369 | — |
| 반응물 | 2-(2-Formyl-3-methoxyphenoxy)acetamide | HCID 42604614 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | 2-[2-(Aminocarbonylmethoxy)-6-methoxyphenyl]-3-(2,6-dimethylphenylamino)-6-fluoroimidazo[1,2-a]pyridine | HCID 24854988 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08258151B2 |
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| 출처 데이터셋 | uspto-grants-2012_09 |
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| ORD ID | ord-df4dd51a7ae14f998fd7e0c33560e0bc |
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| 출처 메모 | uspto-grants-2012_09 |
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