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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 246051생성일: 2026년 10월 25일

Acetic Anhydride → 1-(1H-pyrazolo[4,3-b]pyridin-1-yl)ethanone

https://huagongshe.com/reaction/246051

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Isoamyl NitriteHCID 8053—
반응물Potassium AcetateHCID 517044—
반응물3-Amino-2-methylpyridineHCID 572616—
용매ChloroformHCID 6212—
생성물1-(1H-pyrazolo[4,3-b]pyridin-1-yl)ethanoneHCID 4508621065.3%

반응 단계

To a solution of 3-amino-2-methylpyridine (1.0 g, 9.25 mmol) in CHCl3 (24 ml) at 0° C. was slowly added acetic anhydride (2.0 ml, 21.3 mmol). The reaction mixture was warmed to room temperature and stirred for 1 h. Potassium acetate (272 mg, 2.77 mmol) was added followed by slow addition of isoamyl nitrite (2.7 ml, 19.9 mmol). The reaction mixture was heated at reflux overnight. The reaction mixture was cooled to room temperature and concentrated. The residue was dissolved in EtOAc and washed with water, sat'd NaHCO3 and brine then dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography with 20% to 100% EtOAc/heptane to give 973 mg (65%) of 1-pyrazolo[4,3-b]pyridin-1-yl-ethanone as a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658646B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-4aa0f06762cb497ea0010e80e63bd29b
출처 메모uspto-grants-2014_02