Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 10524-65-9 | HCID 10964417 | — |
| Reactant | HCID 86674845 | HCID 86674845 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 67355881 | HCID 67355881 | 55% |
Reaction Steps
In a 500 ml round bottom flask, methyl 3-(dimethylamino)-2-((dimethylamino)methyleneamino)acrylate (1A, 12 g, 61 mmol) was dissolved in acetic acid (45 ml) and TFA (15 ml). 1,3-Dimethyl-1H-pyrrole (5.8 g, 61 mmol) was added and the mixture was stirred at room temperature for an hour and then at 110° C. for 4 hours. Volatiles were then evaporated from the reaction mixture, the residue was cooled in an ice bath and ice cold saturated K2CO3 solution (200 ml) was slowly added to it. The mixture was extracted with EtOAc (3×250 ml). Combined organic layers were then washed with brine, dried over sodium sulfate, filtered and evaporated. The crude product was purified on a silica column using hexane-EtOAc (0-100%). Desired product methyl 1,3-dimethyl-1H-pyrrolo[3,2-c]pyridine-6-carboxylate (1J, 6.8 g, 55%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403819B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-d331f50568a647939281cd8e4687cb73 |
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| Source note | uspto-grants-2016_08 |
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