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HRID 407368作成日:2026年10月26日

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

https://huagongshe.com/reaction/407368

反応式

関与物質

役割名称HCID仕込み量
反応物Stannous chloride dihydrateHCID 61436—
反応物Ethyl acetate hexaneHCID 21226206—
反応物4-bromo-5-(2-methoxy-5-nitrophenyl)-1-methyl-1H-pyrazoleHCID 23139541—
溶媒EthanolHCID 702—
生成物3-(4-Bromo-1-methyl-1H-pyrazol-5-yl)-4-methoxyanilineHCID 1157274188%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754238B2
出典データセットuspto-grants-2014_06
ORD IDord-7e3b2c91dc9e4451bf5df881a1cfeb1c
出典メモuspto-grants-2014_06