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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64174생성일: 2026년 10월 24일

Nitrogen → N-(3-(3-fluoropyridin-2-yl)-5-nitrophenyl)acetamide

https://huagongshe.com/ko/reaction/64174

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물1,2-DimethoxyethaneHCID 8071—
반응물Sodium CarbonateHCID 10340—
반응물2-Chloro-3-fluoropyridineHCID 2782791—
반응물3-Nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl-acetamideHCID 131737215—
촉매HCID 178477754HCID 178477754—
생성물N-(3-(3-fluoropyridin-2-yl)-5-nitrophenyl)acetamideHCID 8950032170%

반응 단계

A solution of N-(3-nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl-acetamide (10 g, 32.67 mmol) in 1,2-dimethoxyethane (100 ml) was degassed by N2 bubbling for 5 min. 2-Chloro-3-fluoro pyridine (4.29 g, 32.67 mmol) was added and the mixture was degassed for another 5 min. Pd(dppf)cl2 (2.6 g, 3.26 mmol) and aqueous sodium carbonate (10.39 g, 98.03 mmol) were added and the procedure of Example 1(d) was followed. The crude residue of the product was purified by column chromatography (60-120 silica gel, 3% methanol in chloroform) to yield the title product in 70% yield (6.3 g). 1H NMR (300 MHz, DMSO-d6): δ10.64 (s, 1H), 8.74 (m, 1H), 8.62 (m, 1H), 8.55, (brs, 1H), 8.44 (brs, 1H), 7.93 (m, 1H), 7.60 (m, 1H), 2.12 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447091B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-3beae237025b4131ad50a76acee9cc57
출처 메모uspto-grants-2016_09