Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 68539308 | HCID 68539308 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11517531 | HCID 11517531 | 30.3% |
Reaction Steps
Compound 42 (75 mg, 0.17 mmol, 1 equiv) was dissolved in CH2Cl2 (5 mL) and cooled to 0° C. under N2. BBr3 (80 μL, 0.85 mmol, 5 equiv) was added dropwise and the resulting solution was allowed to stir at 0° C. for 2 h. The reaction mixture was then poured into ice and product extracted into EtOAc (250 mL). The organics were washed with saturated aqueous NaCl (100 mL), dried over Na2SO4, filtered and concentrated to dryness. The residue was purified by reverse phase HPLC (0 to 100% CH3CN in water w/0.1% TFA) to provide the title compound (43) (22 mg, 30%) as a tan solid. 1HNMR (400 MHz, DMSO-d6): δ 10.66 (br s, 1H) 10.36 (br s, 1H), 7.87 (s, 1H), 7.57 (m, 1H), 7.32-7.15 (m, 9H), 6.56 (m, 2H), 2.52 (s, 2H), 2.21 (s, 3H). MS m/z 428.5 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07649093B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-c1e2c0b86e784747ae8e1a68d8f34cd0 |
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| Source note | uspto-grants-2010_01 |
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