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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 865672생성일: 2026년 10월 27일

Nitrogen → 2-Acetamido-5-nitropyridine

https://huagongshe.com/reaction/865672

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Acetyl chlorideHCID 6367—
반응물TriethylamineHCID 8471—
반응물2-Amino-5-nitropyridineHCID 77888—
촉매4-(Dimethylamino)pyridineHCID 14284—
생성물2-Acetamido-5-nitropyridineHCID 3451251.5%

반응 단계

To a N2 covered suspension of 3.0 g (21.6 mmol) of 2-amino-5-nitropyridine in 12 ml of CH2C12 was added 9.9 ml (71.2 mmol) of triethylamine followed by 0.13 g (1.1 mmol) of 4-dimethylaminopyridine. The mixture was cooled in an ice bath and there was added 5.06 ml (71.2 mmol) of acetyl chloride dropwise over 18 minutes. The ice bath was removed and after stirring at room temperature for 18 hours, the reaction mixture was diluted with CH2Cl2 and washed once with 20 ml of 1M aqueous K2CO3. The aqueous layer was separated and extracted twice with CH2Cl2. The combined organic fractions were dried over MgSO4 and concentrated in vacuo. The residue was chromatographed over silica gel (20% EtOAc: hexane) and recrystallized from CH3CN to yield 0.653 g, m.p. 196.5°-198° C. (16.7%), 0.157 g, m.p. 183°-193° C. (4.0%) and 0.057 g, m.p. 191°-196° C (1.5%) of the titled product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05567722
출처 데이터셋uspto-grants-1996_10
ORD IDord-6b511dbdfbfd4ffcb7e8cb8fc4d992b7
출처 메모uspto-grants-1996_10