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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 598생성일: 2026년 10월 23일

Tert-butyl cis-(3-carbamoylcyclohexyl)carbamate → tert-butyl N-[(1R,3S)-3-[[5-fluoro-4-(4,5,6,7-tetrahydropyrazolo[1,5-a]pyridin-3-yl)-2-pyridinyl]carbamoyl]cyclohexyl]carbamate

https://huagongshe.com/ko/reaction/598

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참여 물질

역할이름HCID투입량
반응물Tert-butyl cis-(3-carbamoylcyclohexyl)carbamateHCID 71279992—
반응물3-(2-Chloro-5-fluoro-4-pyridinyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridineHCID 124155334—
시약Cesium carbonateHCID 10796—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매1,4-DioxaneHCID 31275—
생성물tert-butyl N-[(1R,3S)-3-[[5-fluoro-4-(4,5,6,7-tetrahydropyrazolo[1,5-a]pyridin-3-yl)-2-pyridinyl]carbamoyl]cyclohexyl]carbamateHCID 12416405637.41%

반응 조건

온도120 °C

반응 단계

Tetrakis(triphenylphosphine)palladium(0) (0.092 g, 0.08 mmol) was added to 3-(2-chloro-5-fluoropyridin-4-yl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine (0.200 g, 0.79 mmol), tert-butyl ((1R,3S)-3-carbamoylcyclohexyl)carbamate (0.231 g, 0.95 mmol) and 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (0.092 g, 0.16 mmol) and Cesium carbonate (0.777 g, 2.38 mmol) in 1,4-dioxane (5.98 ml). Degassed for 5 mins under nitrogen and the resulting suspension was stirred at 120 °C for 2 hours in the microwave reactor. The reaction mixture was partitioned between water (20ml) and DCM (40ml) and separated using a phase separation cartridge. The organics were absorbed onto silica and purified by flash silica chromatography, elution gradient 0 to 60% EtOAc in heptane. Still impure but telescoped through to next stage without further purification. (136mg).

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-c9fc8ca9766b49dfbbd86d67f996e21e
출처 메모750 AstraZeneca ELN dataset