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HRID 18130作成日:2026年10月26日

5-Isocyanato-1,3-dioxaindane → 1-(1,3-benzodioxol-5-yl)-3-{2-[2-(dimethylamino)ethyl]-1,3-dioxo-2,3-dihydro-1H-dibenzo[de,h]isoquinolin-11-yl}urea

https://huagongshe.com/reaction/18130

反応式

関与物質

役割名称HCID仕込み量
反応物5-Isocyanato-1,3-dioxaindaneHCID 5223213—
反応物11-amino-2-[2-(dimethylamino)ethyl]-1H-dibenzo[de,h]isoquinoline-1,3(2H)-dioneHCID 10065413—
反応物Dichloromethane methanolHCID 21226129—
溶媒AcetonitrileHCID 6342—
生成物1-(1,3-benzodioxol-5-yl)-3-{2-[2-(dimethylamino)ethyl]-1,3-dioxo-2,3-dihydro-1H-dibenzo[de,h]isoquinolin-11-yl}ureaHCID 1671787884%

反応条件

温度20 °C

反応手順

A solution of 100 mg (0.30 mmole) of 11-amino-2-[2-(dimethylamino)ethyl]-1H-dibenzo[de,h]isoquinoline-1,3(2H)-dione (obtained in example 3) in 4 mL of acetonitrile was stirred at 20° C. 3,4-(methylenedioxy)phenyl isocyanate (2 molar equivalents) in 3 mL acetonitrile were added. The mixture was magnetically stirred at 20° C. during 18 hours. The solvent was then evaporated under reduced pressure and the residue was submitted to a flash chromatography on silica (eluent: CH2Cl2/methanol in a 95:5 volume ratio) to provide 125 mg (yield: 84%) of the desired product (formula below) as an orange powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741337B2
出典データセットuspto-grants-2010_06
ORD IDord-33b947ef146d494bb67149df97edce5c
出典メモuspto-grants-2010_06