Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1157563생성일: 2026년 10월 25일
Hydrochloric Acid → 2,2,2-Trifluoro-N-{3-[3-(2-{[3-(1,3-oxazol-5-yl)phenyl]amino}-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}acetamide
https://huagongshe.com/reaction/1157563
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 3-(1,3-Oxazol-5-yl)aniline | HCID 2739289 | — |
| 반응물 | N-{3-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}-2,2,2-trifluoroacetamide | HCID 59513717 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 2,2,2-Trifluoro-N-{3-[3-(2-{[3-(1,3-oxazol-5-yl)phenyl]amino}-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}acetamide | HCID 57737242 | 82.2% |
반응 단계
To a solution of N-{3-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}-2,2,2-trifluoroacetamide (1.0 g, 0.002 mol) (see Example 1, Step C) in 1,4-dioxane (25 mL) and i-PrOH (5 mL) was added 3-(1,3-oxazol-5-yl)aniline (1.15 g, 0.007 mols) followed by catalytic 12M HCl. After heating overnight at 90° C., the reaction was quenched with saturated NaHCO3 (25 mL), the solvent was removed by rotary evaporation, the aqueous layer extracted with DCM (25 mL), the organic layer concentrated, and purified by column chromatography (5-50% EtOAc in hexanes then 100% EtOAc) to provide the product (0.89 g, 69%) as an off-white solid. ES-LC/MS m/z=542 [M+H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07807673B2 |
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| 출처 데이터셋 | uspto-grants-2010_10 |
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| ORD ID | ord-28e1c21d1ba34714b8fe488dec9848b5 |
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| 출처 메모 | uspto-grants-2010_10 |
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