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HRID 19558作成日:2026年10月25日

Pyridine → 1-hydroxyimino-3-phenyl-6-(3-phenyl-propoxy)-1H-indene-2-carbonitrile

https://huagongshe.com/reaction/19558

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物1-oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carbonitrileHCID 68695089—
溶媒EthanolHCID 702—
生成物1-hydroxyimino-3-phenyl-6-(3-phenyl-propoxy)-1H-indene-2-carbonitrileHCID 8661403175.6%

反応手順

1-Oxo-3-phenyl-6-(3-phenyl-propoxy)-1H-indene-2-carbonitrile (293 mg, 0.80 mmol) obtained in Example 11 was dissolved in ethanol (20 mL), and hydroxylamine hydrochloride (167 mg, 2.41 mmol) and pyridine (254 mg, 3.21 mmol) were added thereto, refluxed for 3 hrs, and cooled to RT. The resulting mixture washed with saturated sodium bicarbonate, extracted with ethyl acetate. The organic layer was separated, dried over anhydrous MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 230 mg of 1-hydroxyimino-3-phenyl-6-(3-phenyl-propoxy)-1H-indene-2-carbonitrile (yield: 75%). Subsequently, 1-hydroxyimino-3-phenyl-6-(3-phenyl-propoxy)-1H-indene-2-carbonitrile (230 mg, 0.60 mmol) thus obtained was dissolved in methanol (20 mL), and 10%-palladium (230 mg) was added thereto. The mixture was stirred for 15 hrs at RT while providing H2 gas thereto using a balloon, filtered through celite, and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 90 mg of the titled compound (yield: 41%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745439B2
出典データセットuspto-grants-2010_06
ORD IDord-0e82e75908e64cf49e6af380e1135d25
出典メモuspto-grants-2010_06