HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570133Generated: October 26, 2026
2-Isopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → 2-(4-fluorophenyl)-7-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine
https://huagongshe.com/reaction/570133
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Isopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 12727711 | — |
| Reactant | 3-bromo-2-(4-fluorophenyl)-7-methyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine | HCID 89488337 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-fluorophenyl)-7-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine | HCID 89488317 | 44% |
Reaction Steps
To a solution of 3-bromo-2-(4-fluorophenyl)-7-methyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine (1.5 g, 4.82 mmol, 1 eq) in THF (40 ml) is added a solution of n-Buli (3.314 ml, 1.6 M, 5.30 mmol, 1.1 eq) dropwise at −78° C. After 20 min of stirring, a solution of 1.23 g of 2-isopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (7.23 mmol, 1.1 eq) in THF is added dropwise and the reaction mixture is stirred for 2 hours at −78° C. Then the reaction mixture is quenched by the addition of an aqueous solution of NH4Cl and is extracted with EtOAc. The combined organic phases are washed with water and brine, dried over Na2SO4 and concentrated in vacuo. The crude is purified by silica gel chromatography (eluent cyclohexane/ethyl acetate). 760 mg (42%) of 2-(4-fluorophenyl)-7-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine are obtained.
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-8d8bcafc50b3417db0fb46c9e54935ed |
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| Source note | uspto-grants-2015_05 |
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