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HRID 374224作成日:2026年10月25日

Diisopropylethylamine → (S)-7-[3-[[(2,3-Dihydro-7-methoxy-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-one

https://huagongshe.com/reaction/374224

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物7-(3-bromopropoxy)-2H-chromen-2-oneHCID 2757176—
反応物(S)-7-methoxy-2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochlorideHCID 70200787—
溶媒DimethylformamideHCID 6228—
生成物(S)-7-[3-[[(2,3-Dihydro-7-methoxy-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-oneHCID 5412961730.8%

反応条件

温度90 °C

反応手順

(S)-2,3-Dihydro-7-methoxy-1,4-benzodioxin-2-methanamine hydrochloride (11.5 g, 49.8 mmole), 7-(3-bromopropoxy)coumarin (14.2 g, 50.0 mmole), and diisopropylethylamine (12 ml, 68.9 mmole) were combined in 350 ml of DMF and heated at 90° C. for 24 hours uunder a nitrogen atmosphere. The solvent was then removed in vacuum and replaced with 300 ml of dichloromethane. Upon addition of an equal volume of saturated aqueous sodium bicarbonate, a white solid precipitated. This was filtered and redissolved in 550 ml of warm methanol and 35 ml of 4N isopropanolic HCl was added. The solution was boiled on a hot plate and the solvent gradually replaced with isopropanol. Upon cooling, 0.54 g of the title compound precipitated as a white solid, monohydrochloride, quarter hydrate, m.p. 225°-227° C. Subsequent crops yielded as additional 6.1 g of product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05166367
出典データセットuspto-grants-1992_11
ORD IDord-b48187e5953b47e384d8c8619c8a6343
出典メモuspto-grants-1992_11