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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2275115생성일: 2026년 10월 26일

Sodium Thiosulfate → 6,6-Dimethyl-11-oxo-8-(4-oxo-piperidin-1-yl)-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

https://huagongshe.com/reaction/2275115

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ThiosulfateHCID 24477—
반응물Cyclopentyl methyl etherHCID 138539—
반응물Sodium BicarbonateHCID 516892—
반응물8-(4-hydroxypiperidin-1-yl)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrileHCID 54580868—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물6,6-Dimethyl-11-oxo-8-(4-oxo-piperidin-1-yl)-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrileHCID 66834107—

반응 단계

8-(4-Hydroxy-piperidin-1-yl)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile (Compound B2-7-1, 210 mg, 0.545 mmol), was dissolved in the DCM (2 mL) and DMF (0.6 mL) mixture solvent, added with 1,1,1-triacetoxy-1,1-dihydro-1,2-benzoiodoxol-3(1H)-one (300 mg, 1.3 eq.), and the mixture was stirred at room temperature for 2 hr. To the reaction solution, 0.25 mol/L aqueous solution of sodium thiosulfate, saturated sodium bicarbonate solution and CPME were added followed by further stirring at room temperature for 1 hr. The reaction solution was filtered and the filtrate was subjected to liquid separation. The organic layer was washed with saturated brine and dried over sodium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were purified by silica gel column chromatography (ethyl acetate/hexane) to obtain the target compound (yellowish white powder, 109 mg, 52%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09126931B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-5475db352ffc49c999b236e18887603f
출처 메모uspto-grants-2015_09