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HRID 20175作成日:2026年10月23日

Diisopropylamine → 5-(2,3-Difluorophenyl)-1-(2-methoxyethyl)-3-nitropyridin-2(1H)-one

https://huagongshe.com/ja/reaction/20175

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物(2,3-Difluorophenyl)boronic acidHCID 2734333—
反応物Trisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
反応物5-Bromo-1-(2-methoxyethyl)-3-nitropyridin-2(1H)-oneHCID 22293279—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物5-(2,3-Difluorophenyl)-1-(2-methoxyethyl)-3-nitropyridin-2(1H)-oneHCID 2229317359.7%

反応手順

Palladium acetate (41.0 mg, 0.18 mmol) was added to a solution of 5-bromo-1-(2-methoxyethyl)-3-nitropyridin-2(1H)-one (500 mg, 1.81 mmol), 2,3-difluorophenyl boronic acid (570 mg, 3.61 mmol), diisopropylamine (0.759 mL, 5.41 mmol) and 3,3′,3″-phosphinidynetris(benzenesulfonic acid) trisodium salt (310 mg, 0.541 mmol), in N,N-dimethylformamide (15 mL) and water (5 mL) and heated to 80° C. After 2 h, the mixture was allowed to cool to ambient temperature and filtered. Purification by reverse phase HPLC (C-18, 95% water/acetonitrile→5% water/acetonitrile with 0.1% trifluoroacetic acid) gave the title compound (335 mg). MS 311 (M+1). 1H NMR (500 MHz, CDCl3) δ 8.56 (d, J=2.7 Hz, 1H), 8.03 (d, J=2.4 Hz, 1H), 7.23-7.18 (m, 2H), 7.15-7.12 (m, 1H), 4.33 (t, J=4.8 Hz, 2H), 3.74 (t, J=4.8 Hz, 2H), 3.35 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745427B2
出典データセットuspto-grants-2010_06
ORD IDord-603d6f3f4e5349fbacc3acff1172a14e
出典メモuspto-grants-2010_06