돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34544생성일: 2026년 10월 24일

Tetrahydrofuran → 6-chloro-3-methylspiro[1H-quinazoline-4,5'-imidazolidine]-2,2',4'-trione

https://huagongshe.com/ko/reaction/34544

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물TriethylamineHCID 8471—
반응물S-Ethylisothiuronium bromideHCID 200213—
반응물HCID 14229949HCID 14229949—
생성물6-chloro-3-methylspiro[1H-quinazoline-4,5'-imidazolidine]-2,2',4'-trioneHCID 1422996853.1%

반응 단계

5-Chloro-1-methylcarbamoylisatin (4.0 g) is dissolved in tetrahydrofuran (40 ml) and thereto are added 2-ethylisothiourea hydrobromide (4.0 g) and triethylamine (3.0 ml), and the mixture is stirred at room temperature for one hour. The reaction mixture is concentrated under reduced pressure to remove the solvent. To the residue [i.e. 6-chloro- 3-methyl-4-hydroxy-4-(2-ethylisothioureido)carbonyl-2-oxo-1,2,3,4-tetrahydroquinazoline] is added 10% hydrochloric acid (50 ml), and the mixture is stirred at 70°-80° C. for 3 hours. After cooling, the precipitates are taken by filtration to give 6-chloro-3-methyl-spiro[1,2,3,4-tetrahydroquinazoline-4,4'-imidazolidine]-2,2',5'-trione (2.5 g, yield 53.1%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04762839
출처 데이터셋uspto-grants-1988_08
ORD IDord-850eaaccdc6e40e698af6ee15b322d76
출처 메모uspto-grants-1988_08