Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 21713654 | HCID 21713654 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21713650 | HCID 21713650 | — |
Reaction Steps
A dispersion of sodium hydride, 55-60% in oil, (0.0075 g, 0.17 mmol) in dry dimethyl formamide (2 ml) was cooled to −20° C. A solution 2-{3-[3-(3-oxo-3,4-dihydro-quinoxalin-2-yl)-indol-1-yl]-propyl}-isoindol-1,3-dione (0.050 g, 0.11 mmol) in dry dimethyl formamide (2 ml), was added dropwise and the resulting mixture kept at −20° C. for 5 min and then at room temperature for another 15 min. The reaction mixture was cooled to −20° C and methyl iodide (0.017 g, 0.12 mmol, 7.7 μl) was added via a syringe. The resulting solution was allowed to reach room temperature whereupon 12 ml of diethyl ether was added. After 2 h at room temperature, 2-{3-[3-(4-methyl-3-oxo-3,4-dihydro-quinoxalin-2-yl)-indol-1-yl]-propyl}-isoindole-1,3-dione was precipitated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06271231B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-3cd66cf909e0455e8970fceb1aa67b35 |
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| Source note | uspto-grants-2001_08 |
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