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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407368생성일: 2026년 10월 23일

Stannous chloride dihydrate → 3-(4-Bromo-1-methyl-1H-pyrazol-5-yl)-4-methoxyaniline

https://huagongshe.com/ko/reaction/407368

반응식

참여 물질

역할이름HCID투입량
반응물Stannous chloride dihydrateHCID 61436—
반응물Ethyl acetate hexaneHCID 21226206—
반응물4-bromo-5-(2-methoxy-5-nitrophenyl)-1-methyl-1H-pyrazoleHCID 23139541—
용매EthanolHCID 702—
생성물3-(4-Bromo-1-methyl-1H-pyrazol-5-yl)-4-methoxyanilineHCID 1157274188%

반응 단계

To a stirred solution of 4-bromo-5-(2-methoxy-5-nitro-phenyl)-1-methyl-1H-pyrazole (1.799 g, 5.76 mmol) in EtOH (20 mL) was added SnCl2.2H2O (5.306 g, 23.05 mmol, 4.0 eq.), the mixture was stirred at reflux for 2 hrs and EtOH was removed under vacuum. The resulting solid was dissolved in EtOAc, 1N NaOH (30 mL) was added, and the mixture was stirred overnight. The white precipitate was filtered off through celite, and the aqueous phase was extracted with EtOAc (3×80 mL). The combined organic phase was dried over anhydrous MgSO4, filtered and evaporated. The crude reaction mixture was purified by SiO2 column chromatography (Eluent: EtOAc/Hexane=1/3 then 1/1) to give 3-(4-bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenylamine (1.430 g, 5.07 mmol, 88%) as a white solid: LCMS m/z (%)=282 (M+H79Br, 98), 284 (M+H81Br, 100). 1H NMR (400 MHz, CDCl3 (s, 1H), 6.86 (d, J=8.8 Hz, 1H), 6.80 (dd, J=2.8, 8.8 Hz, 1H), 6.22 (d, J=2.4 Hz, 1H), 4.25 (broad s, 2H), 3.72 (s, 3H), 3.71 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754238B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-7e3b2c91dc9e4451bf5df881a1cfeb1c
출처 메모uspto-grants-2014_06