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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1192839생성일: 2026년 10월 23일

N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamine → N-[(6-chloropyridin-3-yl)methyl]-N-(2,2-difluoroethyl)-4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxamide

https://huagongshe.com/ko/reaction/1192839

반응식

참여 물질

역할이름HCID투입량
반응물N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamineHCID 44604123—
반응물Methyl 4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxylateHCID 54677706—
용매ButyronitrileHCID 8008—
생성물N-[(6-chloropyridin-3-yl)methyl]-N-(2,2-difluoroethyl)-4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxamideHCID 86661408—

반응 조건

온도65 °C

반응 단계

10 g of methyl 4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxylate are initially introduced in 111 g of butyronitrile and admixed with 5 g of N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamine. The solution is heated at 65° C. for 3 h. The solution is then extracted with 300 ml of water and then washed with 300 ml of 5% strength hydrochloric acid solution. The organic phase is dried over magnesium sulphate and the solvent is removed in vacuo. For purification, recrystallization from isopropanol is carried out.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08680285B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-33b2f7e565e44cbd870ad14183a7eeae
출처 메모uspto-grants-2014_03