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HRID 234832作成日:2026年10月25日

N,N-Dimethylethylenediamine → 5-[[2-(dimethylamino)ethyl]amino]-2-methylisoquino[5,6,7-cd]indazole-6(2H)-one

https://huagongshe.com/reaction/234832

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylethylenediamineHCID 66053—
反応物5-chloro-2-methylisoquino[5,6,7-cd]indazole-6(2H)-oneHCID 19974770—
生成物5-[[2-(dimethylamino)ethyl]amino]-2-methylisoquino[5,6,7-cd]indazole-6(2H)-oneHCID 19974741—

反応手順

5-chloro-2-methylisoquino[5,6,7-cd]indazole-6 (2H)-one of Example 7 (0.013 g) is added to 2-(dimethylamino)ethylamine (0.34 mL). The yellow mixture is heated quickly to reflux for 1 hour. The excess diamine is removed from the orange solution by a gentle stream of nitrogen. The orange mixture obtained is purified by silica gel column chromatography with a gradient elution (1% methanol/chloroform (25 mL), 2% methanol/chloroform (25 mL), 4% methanol/chloroform (25 mL), 8% methanol/chloroform (25 mL), 12% methanol/chloroform (25 mL), 16% methanol/chloroform (25 mL), 24% methanol/chloroform (50 mL)) to yield 5-[[2-(dimethylamino)ethyl]amino]-2-methylisoquino[5,6,7-cd]indazole-6(2H)-one (0.010 g) as a reddish orange solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05596097
出典データセットuspto-grants-1997_01
ORD IDord-1c9dcf740d32406b9c542abbe30ce882
出典メモuspto-grants-1997_01