Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 3,3-Difluoropyrrolidine hydrochloride | HCID 24903482 | — |
| Reactant | Tert-butyl 9-bromo-2,3-dihydrobenzo[F][1,4]oxazepine-4(5H)-carboxylate | HCID 59403519 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68578493 | HCID 68578493 | 29.8% |
Reaction Steps
A solution of tert-butyl 9-bromo-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (328 mg, 1.04 mmol), 3,3-difluoropyrrolidine hydrochloride (150 mg, 1.04 mmol), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl(X-phos) m (39.8 mg, 0.0835 mmol), tris(dibenzylideneacetone)dipalladium(0) (19.0 mg, 0.0208 mmol) and sodium tert-butoxide (250 mg, 2.60 mmol) in toluene (10 ml) was stirred under an argon atmosphere at 100° C. for 12 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give the desired product (110 mg, 29.8%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247403B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-38efd7ddc2174dd1bbe9ada480357c2e |
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| Source note | uspto-grants-2012_08 |
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