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HRID 916744作成日:2026年10月25日

2-Amino-6-methoxy-3-nitropyridine → HCID 178419698、化合物

https://huagongshe.com/reaction/916744

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-6-methoxy-3-nitropyridineHCID 3852428—
反応物6-Bromo-3-nitro-2-pyridinamineHCID 12097745—
溶媒Acetic Acid Mixture with Hydrobromic AcidHCID 21893785—
生成物HCID 178419698HCID 17841969895%

反応条件

温度60 °C

反応手順

6-Bromo-3-nitro-pyridin-2-ylamine. To a glass pressure vessel containing 6-methoxy-3-nitro-pyridin-2-ylamine (5.0 g, 29.5 mmol) was added 30% hydrogen bromide/acetic acid (60 mL). The vessel was sealed, and the contents were heated to 60° C. for 24 h. The reaction mixture was cooled, and the solvent was removed in vacuo giving 6.8 g (>95%) of crude 6-amino-5-nitro-pyridin-2-ol hydrobromide (HPLC: Rt=5.46). This material (2.0 g, 8.5 mmol) was taken up in toluene (30 mL), followed by phosphorus pentoxide (2.4 g, 17.0 mmol) and tetrabutyl ammonium bromide (3.2 g, 9.7 mmol). The mixture was heated to reflux for 4 h. The reaction mixture was cooled to 0° C., diluted with saturated NaHCO3, and extracted with ethyl acetate (3×100 mL). The combined organics were washed with water (100 mL) and dried (Na2SO4) to afford 1.18 g (64%) of 6-bromo-3-nitro-pyridin-2-ylamine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07271261B2
出典データセットuspto-grants-2007_09
ORD IDord-ef282a0871e9489fae960e26493665f9
出典メモuspto-grants-2007_09