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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225130생성일: 2026년 10월 26일

Water → 2-[4-(7-chloro-4-quinolylamino)phenyl]-N-(1-ethyl-3-piperidyl)acetamide monohydrate

https://huagongshe.com/reaction/225130

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물3-amino-N-ethylpiperidineHCID 98094—
반응물Bis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
반응물2-[4-(7-Chloro-4-quinolylamino)phenyl]acetic acid hydrochlorideHCID 70597336—
용매Dimethyl SulfoxideHCID 679—
생성물2-[4-(7-chloro-4-quinolylamino)phenyl]-N-(1-ethyl-3-piperidyl)acetamide monohydrateHCID 2332900492.5%

반응 조건

온도100 °C

반응 단계

7.0 Grams (0.02 mole) of 2-[4-(7-chloro-4-quinolylamino)phenyl]acetic acid hydrochloride were dissolved in 150 milliliters of dimethyl sulphoxide by heating the stirred mixture to 100° C. under nitrogen. The solution was cooled to room temperature, 6.48 grams (0.04 mole) of carbonyl di-imidazole were added and the mixture was stirred for 21/2 hours under nitrogen. 7.68 Grams (0.06 mole) of 3-amino-1-ethylpiperidine were added, the solution was stirred for another 21/2 hours and poured into 500 milliliters of water. The mixture was refrigerated overnight and the resulting solid was broken up, stirred with water, collected and dried. The solid was dissolved in chloroform and chromatographed on an alumina column made up in chloroform. Elution with chloroform/methanol (4:1) gave 8.15 grams (92.5% yield) of 2-[4-(7-chloro-4-quinolylamino)phenyl]-N-(1-ethyl-3-piperidyl)acetamide monohydrate, melting point 160°-162° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04235908
출처 데이터셋uspto-grants-1980_11
ORD IDord-eb994b99a963498aa299fb5d018646e3
출처 메모uspto-grants-1980_11