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HRID 483232作成日:2026年10月25日

Triethylamine → 3-[2-[4-(2-Methoxyphenyl)-1-piperazinyl]ethyl]-2,4(1H,3H)-quinazolinedione

https://huagongshe.com/reaction/483232

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物DiphosgeneHCID 10426—
反応物Sodium BicarbonateHCID 516892—
反応物1-(2-Methoxyphenyl)-4-[2-(2-aminobenzoyl)-aminoethyl]piperazineHCID 57154715—
溶媒DichloromethaneHCID 6344—
生成物3-[2-[4-(2-Methoxyphenyl)-1-piperazinyl]ethyl]-2,4(1H,3H)-quinazolinedioneHCID 122065—

反応手順

A mixture of 1-(2-methoxyphenyl)-4-[2-(2-aminobenzoyl)-aminoethyl]piperazine (3.54 g) and triethylamine (2.2 g) was dissolved in methylene chloride (50 ml), and the resulting solution was added dropwise to a solution of trichloromethyl chloroformate (0.989 g) in methylene chloride (20 ml) under stirring at between -5° and 5° C. Then, the mixture was gradually heated to room temperature at which it was held for 1 to 2 hours to effect reaction. After completion of the reaction, saturated aqueous sodium hydrogencarbonate was added to the reaction mixture and the resulting mixture was extracted with methylene chloride, the methylene chloride layer was washed with water twice and dried on anhydrous magnesium sulfate. The solvent was concentrated under vacuum and isopropanol was added to the residue to give 2.28 g of crystalline 3-[2-[4-(2-methoxyphenyl)-1-piperazinyl]-ethyl]-2,4-(1H,3H)quinazolinedione having a melting point of 217°-218° C. (recrystallized from chloroform-ether).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04578465
出典データセットuspto-grants-1986_03
ORD IDord-62a9f048b6a045bdbc15ff6899d92e73
出典メモuspto-grants-1986_03