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HRID 517作成日:2026年10月27日

Tert-butyl cis-(3-carbamoylcyclohexyl)carbamate → tert-butyl N-[(1R,3S)-3-[[5-fluoro-4-(5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepin-3-yl)-2-pyridinyl]carbamoyl]cyclohexyl]carbamate

https://huagongshe.com/reaction/517

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl cis-(3-carbamoylcyclohexyl)carbamateHCID 71279992—
反応物3-(2-chloro-5-fluoro-4-pyridinyl)-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepineHCID 124155283—
試薬Cesium carbonateHCID 10796—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒1,4-DioxaneHCID 31275—
生成物tert-butyl N-[(1R,3S)-3-[[5-fluoro-4-(5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepin-3-yl)-2-pyridinyl]carbamoyl]cyclohexyl]carbamateHCID 12416405972.45%

反応条件

温度120 °C

反応手順

Tetrakis(triphenylphosphine)palladium(0) (0.304 g, 0.26 mmol) was added to 3-(2-chloro-5-fluoropyridin-4-yl)-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepine (0.700 g, 2.63 mmol), tert-butyl ((1R,3S)-3-carbamoylcyclohexyl)carbamate (0.638 g, 2.63 mmol) and 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (0.305 g, 0.53 mmol) and Cesium carbonate (2.58 g, 7.90 mmol) in 1,4-dioxane (10 mL)Degassed for 5 mins under nitrogen and the resulting suspension was stirred at 120 °C for 17 hours in the microwave reactor. The reaction mixture was partitioned between water (20ml) and ethyl acetate (100ml) filtered and separated. The organics were absorbed onto silica and purified by flash silica chromatography, elution gradient 1:1 EtOAc in heptane. Pure fractions were evaporated to dryness to afford tert-butyl ((1R,3S)-3-((5-fluoro-4-(5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepin-3-yl)pyridin-2-yl)carbamoyl)cyclohexyl)carbamate (0.900 g, 72.4 %) as a white solid. Product is crude so used directly in the next step.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-5545e57a105549059abb855326d6ce2b
出典メモ750 AstraZeneca ELN dataset