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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 705254생성일: 2026년 10월 24일

1,2-Dichloroethane → tert-butyl (1R,2S,3S,5R)-5-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-2-hydroxy-3-methylcyclohexylcarbamate

https://huagongshe.com/ko/reaction/705254

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물Cesium carbonateHCID 10796—
반응물6-(2,6-Difluorophenyl)-5-fluoropicolinic acidHCID 59226552—
반응물(3aR,5R,7S,7aS)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrobenzo[d]oxazole-3(2H)-carboxylateHCID 90055847—
용매EthanolHCID 702—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물tert-butyl (1R,2S,3S,5R)-5-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-2-hydroxy-3-methylcyclohexylcarbamateHCID 86705216100%

반응 단계

To a solution of (3aR,5R,7S,7aS)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrobenzo[d]oxazole-3(2H)-carboxylate (1.0 equiv.) in DMF (0.2 M) was added 6-(2,6-difluorophenyl)-5-fluoropicolinic acid (1.3 equiv.), aza-HOBt (1.3 equiv.) and EDC (1.3 equiv.). The mixture was stirred at rt for 16 hrs. The solution was diluted with EtOAc, washed with H2O, 1N NaOH, NaCl(sat), dried over MgSO4, filtered and concentrated to yield crude protected amide. The material was dissolved in EtOH (0.45 M), Cs2CO3 (1.0 equiv.) was added and the solution was submerged in a 60° C. oil bath and stirred for 90 mins The volatiles were removed in vacuo; the residue was partitioned between with EtOAc and H2O. The organic layer was washed with NaCl(sat), dried over MgSO4, filtered, concentrated and pumped on to yield tert-butyl (1R,2S,3S,5R)-5-(3-(6-(2,6-difluorophenyl)-5-fluoropicolinamido)pyridin-4-yl)-2-hydroxy-3-methylcyclohexylcarbamate in 100% yield. LC/MS (m/z)=557.3 (MH+), Rt=0.83 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09173883B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-1003449b27584f698c3f27d2a77be4a6
출처 메모uspto-grants-2015_11