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HRID 81993作成日:2026年10月25日

Water → 7-(3,5-dimethyl-4-isoxazolyl)-6-(methyloxy)-N4-[(1R)-1-(2-pyridinyl)ethyl]-3,4-quinolinediamine

https://huagongshe.com/reaction/81993

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium HydroxideHCID 14798—
反応物Stannous ChlorideHCID 24479—
反応物7-(3,5-dimethylisoxazol-4-yl)-6-methoxy-3-nitro-N-((R)-1-(pyridin-2-yl)ethyl)quinolin-4-amineHCID 67207758—
溶媒EthanolHCID 702—
生成物7-(3,5-dimethyl-4-isoxazolyl)-6-(methyloxy)-N4-[(1R)-1-(2-pyridinyl)ethyl]-3,4-quinolinediamineHCID 6720773956%

反応条件

温度40 °C

反応手順

To a suspension of 7-(3,5-dimethylisoxazol-4-yl)-6-methoxy-3-nitro-N—((R)-1-(pyridin-2-yl)ethyl)quinolin-4-amine (Intermediate 24) (1.05 g, 2.503 mmol) in EtOH (20 mL) was added tin(II) chloride (1.66 g, 8.76 mmol) and the mixture stirred at 40° C. for 2.5 h. The reaction mixture was basified to pH 12 using 2M aq. sodium hydroxide solution. Water (30 mL) was added and the aqueous suspension extracted with DCM (3×30 mL). The organic layers were combined, dried by passing through a hydrophobic frit and concentrated to dryness under a stream of nitrogen. The resulting residue was purified by chromatography (100 g column, 2M methanolic ammonia gradient) to give 7-(3,5-dimethylisoxazol-4-yl)-6-methoxy-N4—((R)-1-(pyridin-2-yl)ethyl)quinoline-3,4-diamine (543 mg, 1.39 mmol, 56% yield) as a dark brown gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846709B2
出典データセットuspto-grants-2014_09
ORD IDord-3c6cf0887ec642e7bd1af51ddc2d7ab8
出典メモuspto-grants-2014_09