Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Bromo-1-morpholinophthalazine | HCID 25129478 | — |
| Reactant | HCID 68454361 | HCID 68454361 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 68456522 | HCID 68456522 | — |
Reaction Steps
A 50-mL flask under argon were added 6-bromo-1-morpholinophthalazine (150 mg, 0.51 mmol), 4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide (227 mg, 0.76 mmol), tetrakis(triphenylphosphine)palladium (29 mg, 0.025 mmol), ethyl alcohol (1 mL), and 1,2-dimethoxyethane (4 mL), followed by 2M potassium carbonate aqueous solution (0.77 mL, 1.53 mmol). The reaction was heated at 90° C. for 2 h. The cooled reaction was diluted with CH2Cl2 and washed with saturated aqueous NaHCO3 and brine; dried (MgSO4) and concentrated in vacuo. Trituration of the resulting crude solid with CH2Cl2 afforded a pure batch of the title compound as a white solid. Found MS (ES+): 385.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759337B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-43a30a2de76a4d0c8d9065a360db786d |
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| Source note | uspto-grants-2010_07 |
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