HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → HCID 86597540, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Tributylstannyl)furan | HCID 4393688 | — |
| Reactant | HCID 68687554 | HCID 68687554 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86597540 | HCID 86597540 | — |
Reaction Steps
To a stirring solution of N-(t-butoxycarbonyl)-(R)-1,3,4,10b-tetrahydro-9-trimethylsilylethynyl-7-trifluoromethyl-pyrazino[2,1-a]isoindol-6(2H)-one, prepared according to procedures described in Example 29 with substitution of tributyl(trimethylsilylethynyl)tin for 2-(tributylstannyl)furan (44 mg, 0.1 mmol in MeOH (1.0 mL) was added potassium carbonate (13 mg, 0.1 mmol). The reaction was stirred for 5 min and then quenched with brine. The reaction was extracted with EtOAc (2×5 mL). The organic layers were combined, dried over Na2SO4, and conc. in vacuo to a pale yellow oil. The oil was purified by radial chromatography (silica gel, 30% EtOAc in hexanes) to give 27 mg of the desired-product as a pale yellow oil. MS (ESI) 381 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244843B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-f1bf1bedc3ff4472a0d8b5182adc9c6c |
| Source note | uspto-grants-2007_07 |