Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 86651379 | HCID 86651379 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 50991463 | HCID 50991463 | — |
Reaction Steps
N-Bromosuccinimide (8.1 mg, 0.046 mmol) was added to a mixture solution of tert-butyl 4-(1-(pyridin-4-yl)-1H-indol-6-yl)phenol (10 mg, 0.035 mmol) in THF (0.5 mL) mixture solution at −78° C. After stirring at −78° C. for 2 hours, the mixture was further stirred at 0° C. for 1 hour and then pyridine (8.5 μL, 0.105 mmol) was added. After stirring at room temperature for 30 minutes, water was added and the mixture was extracted with ethyl acetate. The collected organic layer was washed with saturated sodium bicarbonate solution and brine, and then concentrated under reduced pressure by drying with anhydrous magnesium sulfate. The target compound was obtained as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329708B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-a9a7879b337c4f608e1b0ae98082c994 |
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| Source note | uspto-grants-2012_12 |
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