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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2272691생성일: 2026년 10월 26일

Ammonium Chloride → N2-(3-Fluoro-4-methylphenyl)pyridine-2,3-diamine

https://huagongshe.com/reaction/2272691

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물N-(3-fluoro-4-methylphenyl)-3-nitro-2-pyridylamineHCID 40676958—
촉매ZincHCID 23994—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물N2-(3-Fluoro-4-methylphenyl)pyridine-2,3-diamineHCID 29067357110.9%

반응 단계

Zinc dust (14.3 g, 219 mmol) was added to a stirring mixture of N-(3-fluoro-4-methylphenyl)-3-nitropyridin-2-amine (C1) (6.78 g, 27.4 mmol) and ammonium chloride (11.7 g, 219 mmol) in tetrahydrofuran (55 mL) and water (55 mL), which caused the temperature of the mixture to rise to 45° C. The reaction mixture was stirred for 10 minutes, and then filtered through a pad of Celite, rinsing with ethyl acetate. The organic layer from the filtrate was further diluted with ethyl acetate, washed with aqueous ammonium chloride solution and with saturated aqueous sodium chloride solution, dried over magnesium sulfate, and filtered. The filtrate was concentrated in vacuo to afford the product as a black solid (6.6 g), the bulk of which was taken directly to the following step. LCMS m/z 218.1 [M+H]+. 1H NMR (400 MHz, CDCl3), characteristic product peaks: δ 7.84 (dd, J=4.9, 1.6 Hz, 1H), 7.01 (dd, J=7.6, 1.6 Hz, 1H), 6.82 (br dd, J=8, 2 Hz, 1H), 6.77 (dd, J=7.6, 4.9 Hz, 1H), 2.20 (d, J=2 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09120788B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-45ced77ae4694299a580cf8281ae971c
출처 메모uspto-grants-2015_09