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HRID 1900716作成日:2026年10月27日

2-Azidomethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-one → 2-Aminomethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-one

https://huagongshe.com/reaction/1900716

反応式

関与物質

役割名称HCID仕込み量
反応物2-Azidomethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-oneHCID 23369718—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒DimethylformamideHCID 6228—
生成物2-Aminomethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-oneHCID 23369567102.6%

反応手順

2-Azidomethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-one (759 mg) was dissolved in dimethylformamide (20 ml). To the solution, 10% palladium-on-carbon (455 mg) was added, and the solution was hydrogenated in the atmosphere of hydrogen at ambient temperature and under atmospheric pressure. After completion of the reaction, the catalyst was filtered off. When the solvent was evaporated, 0.7 g of the title compound was obtained as a crude product. This product was purified by silica gel column chromatography to obtain 409 mg of a free base (60.0%). The obtained free base was converted into a hydrochloric acid salt, followed by recrystallizing from a solvent mixture of methanol-diethylether, obtaining yellow powdery crystals having a melting point over 300° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05576324
出典データセットuspto-grants-1996_11
ORD IDord-071ca108d66c46a7856cd12d5b1c6ef7
出典メモuspto-grants-1996_11