Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 5-Methoxy-4-aza-2-oxindole | HCID 10773321 | — |
| Product | HCID 21931746 | HCID 21931746 | — |
Reaction Steps
A solution of 0.2 g (1.22 mmol) 5-methoxy-1,3-dihydro-pyrrolo[3,2-b]pyridin-2-one (J. Het. Chem. 1996, 33, 287–93) was dissolved in 10 ml of DMF and cooled to 0° C. under a nitrogen atmosphere in a flame dried round bottom flask. To this solution was added 4.02 ml (4.02 mmol) of a 1M solution of potassium t-butoxide in THF and the solution was stirred for 10 minutes. To this solution was added dropwise 0.3 ml (4.88 mmol) of MeI, and the reaction was stirred for 15 minutes at 0° C. The reaction was quenched with water and extracted with ethyl acetate. The ethyl acetate extracts were dried (Na2SO4) and evaporated. The residue was chromatographed on 6 g of silica using 3:1 hexanes/ethyl acetate as the elutant. Appropriate fractions were combined and evaporated to yield 0.14 g of 5-methoxy-1,3,3-trimethyl-1,3-dihydro-pyrrolo[3,2-b]pyridin-2-one. 1H NMR (CDCl3) δ 7.02 (d, 1H), 6.58 (d, 1H), 3.90 (s, 3H), 3.18 (s, 3H), 1.38 (s, 6H). Mass spectrum: m/e=207 (P+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119207B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-aec85dda45e242fe9ed1f9491cd08475 |
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| Source note | uspto-grants-2006_10 |
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