HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586899Generated: November 2, 2026
Potassium Carbonate → HCID 22329078, compound
https://huagongshe.com/reaction/586899
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-bromo-1-methyl-N-[4-[[N-methyl-N-(tetrahydropyran-4-yl)amino]methyl]phenyl]-2,3-dihydro-1-benzoazepine-4-carboxamide | HCID 22329036 | — |
| Reactant | HCID 86756787 | HCID 86756787 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ethanol toluene water | HCID 86587398 | — |
| Product | HCID 22329078 | HCID 22329078 | 49% |
Reaction Steps
In a mixture of water:ethanol:toluene (1:1:10, v/v, 18.0 ml) were dissolved (2,3-dihydro-1,4-benzodioxin-6-yl)borate (221 mg) and 7-bromo-1-methyl-N-[4-[[N-methyl-N-(tetrahydro-2H-pyran-4-yl)amino]methyl]phenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxamide (397 mg). To the solution was added potassium carbonate (272 mg), and the mixture was stirred under argon atmosphere at room temperature for 30 minutes. To the mixture was added tetrakistriphenylphosphinepalladium (38 mg), and the mixture was heated to reflux under argon atmosphere for 10 hours. The mixture was diluted with ethyl acetate, and washed with water and saturated brine, and the organic layer was dried with anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified with silica gel column chromatography (35 g, ethyl acetate:ethanol=20:1) and recrystallized from ethanol to give 7-(2,3-dihydro-1,4-benzodioxin-6-yl)-1-methyl-N-[4-[[N-methyl-N-(tetrahydro-2H-pyran-4-yl)amino]methyl]phenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxamide (Compound 24) (215 mg, 49%) as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936602B1 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-dc7da52c713342598d47300e978a4309 |
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| Source note | uspto-grants-2005_08 |
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