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HRID 18138作成日:2026年10月24日

Triethylamine → 4-fluorophenyl {2-[2-(dimethylamino)ethyl]-1,3-dioxo-2,3-dihydro-1H-dibenzo[de,h]isoquinolin-11-yl}carbamate

https://huagongshe.com/ja/reaction/18138

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Fluorophenyl chloroformateHCID 2733256—
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DichloromethaneHCID 6344—
生成物4-fluorophenyl {2-[2-(dimethylamino)ethyl]-1,3-dioxo-2,3-dihydro-1H-dibenzo[de,h]isoquinolin-11-yl}carbamateHCID 1671793572.8%

反応条件

温度20 °C

反応手順

100 mg of 11-amino-2-[2-(dimethylamino)ethyl]-1H-dibenzo[de,h]isoquinoline-1,3(2H)-dione (obtained in example 3) (0.30 mmol) were dissolved in 6 ml of dichloromethane. 85 μl (2 molar equivalents) of triethylamine and 105 mg (2 molar equivalents) of 4-fluorophenyl chloroformate were respectively added. The reaction mixture was maintained at 20° C. for 3 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 103 mg (yield=66%) 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-c94d88cca3d44cde873ed04a9b63fa98
出典メモuspto-grants-2010_06