HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570134Generated: October 26, 2026
Sodium Carbonate → HCID 89488325, compound
https://huagongshe.com/reaction/570134
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | tert-butyl N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)carbamate | HCID 49760449 | — |
| Reactant | HCID 89488351 | HCID 89488351 | — |
| Catalyst | Bis(tricyclohexylphosphine)palladium(II) Dichloride | HCID 11556747 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 89488325 | HCID 89488325 | — |
Reaction Steps
3-bromo-2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine (700 mg, 2.25 mmol) and tert-butyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]carbamate (792 mg, 2.47 mmol, 1.1 eq) are dissolved in 10 mL 1,4-dioxan. To this mixture Bis(tricyclohexylphosphine)palladium(II)-dichloride (166 mg, 0.22 mmol, 0.1 eq) and 5.4 mL sodium carbonate solution (2 molar) are added. The reaction mixture is flushed with argon for 5 mins and then sealed. Next the mixture is heated for 12 mins at 150° C. in the microwave (Biotage). The procedure is repeated 7× using the same scale and all crude reaction mixtures are combined thereafter. After cooling, insoluble components are filtered off over Celite and the residue washed with 1,4-dioxan. The organic phase is evaporated and the crude product purified by column chromatography over silica gel using dichloromethane/methanole as eluent. After evaporation of the solvents 2.10 g (41%) of 4-(2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazin-3-yl)pyridin-2-amine are obtained as a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023844B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-aebb6ad8c982489ba5f1b5cc6e4075ef |
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| Source note | uspto-grants-2015_05 |
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