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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1613124생성일: 2026년 10월 26일

Methanol → 5-[5-(N-acetyl-anilino)-2, 3-pentadienylidene]-2,7-diphenyl-4-methylpyrazolo[3,4-b]pyridine-3,6-dione

https://huagongshe.com/reaction/1613124

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물TriethylamineHCID 8471—
반응물N-(5-(phenylamino)penta-2,5-dienylidene)aniline monohydrochlorideHCID 73902—
반응물4-methyl-2,7-diphenyl-1H-pyrazolo[3,4-b]pyridine-3,6-dioneHCID 360316—
용매Acetic AcidHCID 176—
생성물5-[5-(N-acetyl-anilino)-2, 3-pentadienylidene]-2,7-diphenyl-4-methylpyrazolo[3,4-b]pyridine-3,6-dioneHCID 57123698—

반응 단계

A solution was prepared by adding 50 ml of methanol and 2.8 ml of triethylamine to 3.17 g of 2,7-diphenyl-4-methylpyrazolo[3, 4-b]pyridine-3,6-dione, and 2.85 g of 1,7-diphenyl-1,7-diaza-1,3,5-heptatriene hydrochloride was added to this solution, followed by the addition of 1.88 ml of anhydrous acetic acid and stirring at room temperature for 1 hour. The precipitate thus formed was filtered and washed with methanol, followed by drying, to obtain 1.9 g of 5-[5-(N-acetyl-anilino)-2, 3-pentadienylidene]-2,7-diphenyl-4-methylpyrazolo[3,4-b]pyridine-3,6-dione. 60 ml of N,N-dimethylformamide, 0.95 g of 2,7-diphenyl-4-methylpyrazolo[3,4-b]pyridine-3,6-dione and 0.42 ml of triethylamine were added to 1.5 g of this product, and the mixture was stirred at 50° C. for two hours. After filtering off a trace amount of the insoluble matter, ethyl acetate in an amount of ten times by volume was added to precipitate crystals while stirring. The obtained crystals were dissolved again in a small amount of N,N-dimethylformamide, and ethyl acetate in an amount of ten times by volume was added to precipitate crystals, followed by filtering and drying the crystals, whereby 1.3 g of Compound 2 were obtained. Golden crystal. Melting point: 300° C. or higher.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05192738
출처 데이터셋uspto-grants-1993_03
ORD IDord-e1ccbd1618a34a62af6ddff7fd4a222e
출처 메모uspto-grants-1993_03