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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19558생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/19558

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물1-oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carbonitrileHCID 68695089—
용매EthanolHCID 702—
생성물1-hydroxyimino-3-phenyl-6-(3-phenyl-propoxy)-1H-indene-2-carbonitrileHCID 8661403175.6%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745439B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0e82e75908e64cf49e6af380e1135d25
출처 메모uspto-grants-2010_06