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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamine | HCID 44604123 | — |
| 반응물 | Methyl 4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxylate | HCID 54677706 | — |
| 용매 | Butyronitrile | HCID 8008 | — |
| 생성물 | N-[(6-chloropyridin-3-yl)methyl]-N-(2,2-difluoroethyl)-4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxamide | HCID 86661408 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08680285B2 |
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| 출처 데이터셋 | uspto-grants-2014_03 |
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| ORD ID | ord-33b2f7e565e44cbd870ad14183a7eeae |
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| 출처 메모 | uspto-grants-2014_03 |
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