Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1874407생성일: 2026년 10월 26일
Trifluoroacetic anhydride → N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]-5-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide
https://huagongshe.com/reaction/1874407
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Trifluoroacetic anhydride | HCID 9845 | — |
| 반응물 | N-{3-[(1-(2-amino-2-oxoethyl)-6-{[(4-methylphenyl)sulfonyl]imino}-1,6-dihydropyridin-3-yl)oxy]-5-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide | HCID 68987360 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]-5-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide | HCID 57749097 | 56% |
반응 단계
A mixture of N-{3-[(1-(2-amino-2-oxoethyl)-6-{[(4-methylphenyl)sulfonyl]imino}-1,6-dihydropyridin-3-yl)oxy]-5-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide (3.20 g, 5.82 mmol), trifluoroacetic anhydride (20 mL) and dichloromethane (30 mL) was stirred at room temperature for 4 hr. The reaction solution was concentrated under reduced pressure, ethanol (30 mL), water (15 mL) and 8N aqueous sodium hydroxide solution (15 mL) were added to the residue, and the mixture was stirred at room temperature for 60 hr. The reaction solution was concentrated under reduced pressure and ethyl acetate was added to the residue. The mixture was washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was collected by filtration and washed with diethyl ether to give the title compound (1.22 g, 56%) as a pale-brown solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08304557B2 |
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| 출처 데이터셋 | uspto-grants-2012_11 |
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| ORD ID | ord-6b0b17adc56d4beebdd3c69b3441f3ce |
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| 출처 메모 | uspto-grants-2012_11 |
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