돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 483232생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/483232

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DiphosgeneHCID 10426—
반응물Sodium BicarbonateHCID 516892—
반응물1-(2-Methoxyphenyl)-4-[2-(2-aminobenzoyl)-aminoethyl]piperazineHCID 57154715—
용매DichloromethaneHCID 6344—
생성물3-[2-[4-(2-Methoxyphenyl)-1-piperazinyl]ethyl]-2,4(1H,3H)-quinazolinedioneHCID 122065—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04578465
출처 데이터셋uspto-grants-1986_03
ORD IDord-62a9f048b6a045bdbc15ff6899d92e73
출처 메모uspto-grants-1986_03