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 | US08802695B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-b87f9432d7cf43f0a99696dc09816efd |
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| Source note | uspto-grants-2014_08 |
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