돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51971생성일: 2026년 10월 23일

Hydrochloric Acid → Ethyl 7-aminoquinoline-3-carboxylate

https://huagongshe.com/ko/reaction/51971

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물7-(Benzhydrylidene-amino)-quinoline-3-carboxylic acid ethyl esterHCID 10287230—
용매EthanolHCID 702—
생성물Ethyl 7-aminoquinoline-3-carboxylateHCID 987780168.3%

반응 단계

Concentrated hydrochloric acid (1 mL, 2.5 volumes) was added to a solution of 7-(benzhydrylidene-amino)-quinoline-3-carboxylic acid ethyl ester (400 mg, 1.05 mmol, 1 equiv) in ethanol (4 mL, 10 volumes). The solution was stirred at room temperature for three hours and then concentrated. The residue was dissolved in ethyl acetate (20 mL, 50 volumes) and the organic layer was washed with 1 N hydrochloric acid (5×25 mL). The pH of the combined aqueous layer was then adjusted to about 8 with solid sodium hydroxide. The aqueous layer was then extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over sodium sulfate and concentrated to provide 7-amino-quinoline-3-carboxylic acid ethyl ester (155 mg, 68%) as a yellow solid. The crude solid can be further purified by flash column chromatography using silica gel (EM Science, Gibbstown, N.J., 230-400 mesh) in 60% ethyl acetate in hexanes if desired.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713489B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-194726897d924469839c471fea67f027
출처 메모uspto-grants-2004_03