Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 69017489 | HCID 69017489 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57941176 | HCID 57941176 | — |
Reaction Steps
To a flask equipped with stir bar was added benzyl 4-(2,5-difluorophenyl)-6-(3-methoxyphenyl)-3,6-dihydropyridine-1(2H)-carboxylate (1-4, 0.51 g, 1.17 mmol) and dichloromethane (20 mL). The resulting solution was cooled to 0° C. and treated with BBr3 (0.15 mL, 1.17 mmol). The reaction was stirred at 0° C. for 4 h, then warmed to 23° C. Upon completion, the reaction was diluted with dichloromethane (100 mL) and washed with water (3×100 mL). The organics were dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was carried into the subsequent acylation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622489B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-bb3f8cff3cbb495bb7b5536eef140e69 |
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| Source note | uspto-grants-2009_11 |
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