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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 705306생성일: 2026년 10월 24일

Methane → tert-butyl (3R,4S,5S)-1-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-5-methyl-4-(4-methyl-1H-1,2,3-triazol-1-yl)piperidin-3-ylcarbamate

https://huagongshe.com/ko/reaction/705306

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물PropyneHCID 6335—
반응물TriethylamineHCID 8471—
반응물tert-butyl (3R,4S,5S)-4-azido-1-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-5-methylpiperidin-3-ylcarbamateHCID 86705273—
촉매CopperHCID 23978—
용매1,4-DioxaneHCID 31275—
생성물tert-butyl (3R,4S,5S)-1-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-5-methyl-4-(4-methyl-1H-1,2,3-triazol-1-yl)piperidin-3-ylcarbamateHCID 8670527495%

반응 조건

온도60 °C

반응 단계

In a high pressure vial was added tert-butyl (3R,4S,5S)-4-azido-1-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-5-methylpiperidin-3-ylcarbamate (1.0 equiv.), copper in charcoal (0.2 equiv.), prop-1-yne (10.0 equiv.) and triethylamine (1.5 equiv.), in dioxane (0.15 M) to give a black suspension. The pressure tube was sealed and the mixture was stirred with heating to 60° C. for 48 hrs. The reaction was cooled to RT, filtered through celite, concentrated to yield tert-butyl (3R,4S,5S)-1-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-5-methyl-4-(4-methyl-1H-1,2,3-triazol-1-yl)piperidin-3-ylcarbamate in 95% yield. LC/MS (m/z)=623.2 (MH+), Rt=0.87 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09173883B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-388ee90852a24677975f1d120ce19cdf
출처 메모uspto-grants-2015_11