HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978758Generated: October 30, 2026
Potassium Carbonate → HCID 70244587, compound
https://huagongshe.com/reaction/1978758
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-bromo-N-[4-[[N-methyl-N-(tetrahydropyran-4-yl)amino]methyl]phenyl]-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxamide | HCID 21995706 | — |
| Reactant | Ethanol toluene water | HCID 86587398 | — |
| Reactant | HCID 86756843 | HCID 86756843 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70244587 | HCID 70244587 | 28.6% |
Reaction Steps
To 7-bromo-N-[4-[[N-methyl-N-(tetrahydropyran-4-yl)amino]methyl]phenyl]-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxamide (0.35 g) was added toluene/ethanol/water (10/1/1,16.3 ml) and then were added 2-methyl-1,3-benzoxazol-5-yl borate (0.14 g) and potassium carbonate (0.23 g), and the mixture was stirred at room temperature for 30 minutes. To the mixture was added tetrakistriphenylphosphinepalladium (31 mg), and the mixture was refluxed for 14 hours, cooled to room temperature, poured into water. The mixture was extracted with ethyl acetate, washed with saturated brine and dried with magnesium sulfate. Under reduced pressure, the solvent was removed, and the residue was purified with silica gel column chromatography (ethyl acetate/ethanol=4/1) and recrystallized from ethanol to give 7-(2-methyl-1,3-benzoxazol-5-yl)-N-[4-([N-methyl-N-(tetrahydropyran-4-yl)amino]methyl]phenyl]-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxamide (Compound 135) (110 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06235771B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-d077c171d1c143f3b3416fc931dbf48a |
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| Source note | uspto-grants-2001_05 |
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