Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | HCID 23734890 | HCID 23734890 | — |
| Reactant | 3-Bromo-5-(morpholin-4-yl)-7H-thieno[3,2-b]pyran-7-one | HCID 44181178 | — |
| Catalyst | CID 53485975 | HCID 53485975 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 44180968 | HCID 44180968 | — |
Reaction Steps
A 2 mL microwave vial was charged with a magnetic stirring bar, 2-morpholinoethyl 4-iodobenzoate (90 mg, 249 μmol), 3-bromo-5-morpholino-7H-thieno[3,2-b]pyran-7-one (103) (79 mg, 249 μmol), bis(pinacolato)diboron (70 mg, 274 gmol), cesium carbonate (325 mg, 997 dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (6 mg, 7 μmol), and 1,2-dimethoxyethane (1 mL). The reaction mixture was sealed, and the reaction mixture was magnetically stirred and heated under microwave irradiation to 140° C. for 15 minutes to give 2-morpholinoethyl 4-(5-morpholino-7-oxo-7H-thieno[3,2-b]pyran-3-yl)benzoate (77).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557807B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-59e1b641745047f5ad18fa76b763278d |
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| Source note | uspto-grants-2013_10 |
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