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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 475021생성일: 2026년 10월 25일

Acetohydroxamic Acid → 5-(4-amino-1-isopropyl-1H-pyrazolo[4,3-c]pyridin-3-yl)benzo[d]isoxazol-3-amine

https://huagongshe.com/reaction/475021

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참여 물질

역할이름HCID투입량
반응물Acetohydroxamic AcidHCID 1990—
반응물DimethylformamideHCID 6228—
반응물Potassium tert-butoxideHCID 23665647—
반응물5-(4-amino-1-isopropyl-1H-pyrazolo[4,3-c]pyridin-3-yl)-2-fluorobenzonitrileHCID 58209112—
생성물5-(4-amino-1-isopropyl-1H-pyrazolo[4,3-c]pyridin-3-yl)benzo[d]isoxazol-3-amineHCID 4420375955%

반응 조건

온도25 °C

반응 단계

A mixture of 5-(4-amino-1-isopropyl-1H-pyrazolo[4,3-c]pyridin-3-yl)-2-fluorobenzonitrile (304) (49 mg, 0.166 mmol), N-hydroxyacetamide (compound 305) (18.7 mg, 1.5 eq, 0.249 mmol) and t-BuOK (27.9 mg, 1.5 eq, 0.249 mmol) in DMF (4 mL) was stirred at 25° C. overnight. The mixture was concentrated in vacuo, brine (10 mL) was added and then extracted with ethyl acetate (3×30 mL). The combined organic layer was washed with brine (10 mL), dried over MgSO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by flash column chromatography eluting with a mixture of methanol in dichloromethane to afford the desired product, 5-(4-amino-1-isopropyl-1H-pyrazolo[4,3-c]pyridin-3-yl)benzo[d]isoxazol-3-amine (7) (28 mg, 55% yield) (compound 306) as a white solid. ESI-MS m/z: 309.35 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637542B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-2d6baf214b3a4cde87818f87d6c19b21
출처 메모uspto-grants-2014_01