돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1749070생성일: 2026년 10월 26일

Ethyl 3,3,3-trifluoro-2-oxopropanoate → Tert-butyl 4-(3-oxo-2-(trifluoromethyl)-3,4-dihydropyrido[2,3-b]pyrazin-8-yloxy)naphthalen-1-ylcarbamate

https://huagongshe.com/reaction/1749070

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 3,3,3-trifluoro-2-oxopropanoateHCID 2737239—
반응물Tert-butyl 4-(2,3-diaminopyridin-4-yloxy)naphthalen-1-ylcarbamateHCID 44186229—
용매EthanolHCID 702—
생성물Tert-butyl 4-(3-oxo-2-(trifluoromethyl)-3,4-dihydropyrido[2,3-b]pyrazin-8-yloxy)naphthalen-1-ylcarbamateHCID 46900749—

반응 단계

To tert-butyl 4-(2,3-diaminopyridin-4-yloxy)naphthalen-1-ylcarbamate (1.00 g, 2.73 mmol) dissolved in 20 mL of anhydrous ethanol under argon and at reflux was added the ethyl trifluoropyruvate (697 mg, 0.50 mL, 4.10 mmol). The reaction mixture was stirred at reflux for 3 hours. After cooling at RT, a precipitate was formed, filtered off and rinsed with Et2O. tert-butyl 4-(3-oxo-2-(trifluoromethyl)-3,4-dihydropyrido[2,3-b]pyrazin-8-yloxy)naphthalen-1-ylcarbamate was obtained as a white solid (116 mg, 0.246 mmol, 9%). The filtrate was evaporated under vacuum. The residue was chromatographied (eluent: CH2Cl2/EtOAc: 4/1 towards 0/1) to afford the second isomer as a slightly yellow solid (540 mg, 1.14 mmol, 42%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09155737B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-a3de033e9846403c98f36492057ebdf3
출처 메모uspto-grants-2015_10