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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 609764생성일: 2026년 10월 24일

Potassium Hydroxide → 1-benzyl-6-chloro-2-(3,4-dihydro-2(1H)-quinolinon-6-ylaminocarbonyl)benzimidazole

https://huagongshe.com/ko/reaction/609764

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물6-amino-3,4-dihydroquinolin-2(1H)-oneHCID 4912759—
반응물HCID 19600410HCID 19600410—
반응물Aluminium lithium hydrideHCID 21226445—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-benzyl-6-chloro-2-(3,4-dihydro-2(1H)-quinolinon-6-ylaminocarbonyl)benzimidazoleHCID 196003977.7%

반응 단계

130 Milligrams of lithium aluminum hydride was suspended in 70 ml of tetrahydrofuran, then 2.2 g of 6-amino-3,4-dihydro-2(1H)-quinolinone was added gradually thereto, and the mixture was stirred at room temperature overnight. The reaction mixture was further stirred for 2 hours under refluxing condition, then 1 g of methyl 1-benzyl-6-chlorobenzimidazol-2-carboxylate was added, the reaction was continued by refluxing for 3 hours. After the reaction was finished, then water and 10% aqueous solution of potassium hydroxide were added, the reaction mixture was diluted with ethyl acetate and filtered with Celite, and the filtrate was washed with chloroform, the solvent was removed by distillation under reduced pressure. To the residue thus obtained was added ethanol and heated, the insoluble matters were collected by filtration and recrystallized from dimethylformamide, there was obtained 0.11 g of 1-benzyl-6-chloro-2-(3,4-dihydro-2(1H)-quinolinon-6-ylaminocarbonyl)benzimidazole as in the form of yellow powdery product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05998437
출처 데이터셋uspto-grants-1999_12
ORD IDord-0e5e2ed8966e43c7bda8a29c12937834
출처 메모uspto-grants-1999_12