Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloropyrazine | HCID 73277 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 4-Bromoindole | HCID 676494 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-pyrazin-2-yl-1H-indole | HCID 68717665 | — |
Reaction Steps
4-Bromoindole (0.1 g, 0.51 mmol), bis(pinacolato)diboron (0.172 g, 0.77 mmol), potassium acetate (0.075 g, 0.765 mmol) and PdCl2 (0.022 g, 0.031 mmol) were dissolved in DME (3 mL) and heated in the microwave for 900 seconds at 125° C. The reaction was cooled and NaHCO3 (0.129 g, 1.53 mmol), 2-chloropyrazine (0.087 g, 0.77 mmol) tetrakis(triphenylphosphine)palladium (0.0295 g, 0.026 mmol), H2O (1 mL) and DME (1 mL) were added and the mixture was stirred in the microwave for 900 seconds at 120° C. The mixture was diluted with dichloromethane and filtered. The filtrate was washed with water (2×), dried (MgSO4) and evaporated. The crude product was purified by flash chromatography using 2.5% to 5% CH3OH in dichloromethane. Not pure, purified by flash chromatography using hexane/EtOAc 7:3 to 1:1 as the eluent. Yield: 93 mg (47%). White solid. MS (electronspray; [M+H]+) m/z 196.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812017B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-fe6fd4cded794428afabcbe8cad33f60 |
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| Source note | uspto-grants-2010_10 |
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