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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53441생성일: 2026년 10월 25일

Formic Acid → Cyclopropanecarboxamido-4-methyl-3-nitropyridine

https://huagongshe.com/reaction/53441

반응식

참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물TriethylamineHCID 8471—
반응물2-cyclopropanecarboxamido-5-Bromo-4-Methyl-3-nitropyridineHCID 10979482—
촉매PalladiumHCID 23938—
용매TolueneHCID 1140—
생성물Cyclopropanecarboxamido-4-methyl-3-nitropyridineHCID 1538088572.3%

반응 단계

Toluene (60 ml) was added to 3.0 g (10.0 mmol) of 5-bromo-2-cyclopropanecarboxamido-4-methyl-3-nitropyridine, 10% Pd-C (100 mg) and 2.9 g (28.6 mmol) of triethylamine, followed by stirring and heating under reflux. 1.9 g (41.3 mmol) of formic acid was dropwise added to this solution, followed by stirring for 5 hours. The reaction liquid was brought to room temperature and filtered to remove the catalyst. The filtrate was subjected to vacuum concentration. Chloroform (100 ml) and water (100 ml) were added to the residue and the obtained mixture was caused liquid-liquid separation. The aqueous phase was further extracted with chloroform (50 ml) once. The organic phases were combined, dried over anhydrous magnesium sulfate and subjected to vacuum concentration. The residue was purified by silica gel column chromatography (a n-hexane/ethyl acetate system) to give 1.6 g of the title compound (yield 72%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618969
출처 데이터셋uspto-grants-1997_04
ORD IDord-868eab46688c4b149fd7a79c0d17fd8d
출처 메모uspto-grants-1997_04