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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1414880생성일: 2026년 10월 26일

2-Chloroquinoline-4-carbonyl chloride → 2-Chloro-N-(1-cyclohexylpyrrolidin-3-yl)quinoline-4-carboxamide

https://huagongshe.com/reaction/1414880

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloroquinoline-4-carbonyl chlorideHCID 75438—
반응물1-Cyclohexylpyrrolidin-3-amineHCID 3670074—
용매ChloroformHCID 6212—
생성물2-Chloro-N-(1-cyclohexylpyrrolidin-3-yl)quinoline-4-carboxamideHCID 20355405—

반응 단계

To 3.16 gm. (0.0195mole) of 3-amino-1-cyclohexylpyrrolidine in 50 ml. of chloroform was added dropwise a solution of 3.5 gm. (0.015 mole) of 2-chloro-4-quinolinecarbonyl chloride in 50 ml. of chloroform. The reaction mixture was concentrated under reduced pressure and the residue was partitioned between ethyl acetate containing 10% isopropyl ether and dilute hydrochloric acid. The separated acid layer was made basic with dilute sodium hydroxide solution and extracted with chloroform. The chloroform solution was dried over sodium sulfate, concentrated and the residue recrystallized twice from isopropyl ether-ethyl acetate. The product (0.7 gm.; 13%) melted at 127°-219° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04002757
출처 데이터셋uspto-grants-1977_01
ORD IDord-87f00d114d904ee19aa0f48fa78ae185
출처 메모uspto-grants-1977_01