HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium ethoxide → ethyl 3-amino-1H-pyrrolo[3,2-c]pyridine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl-4-(3-cyanopyridine)glycinate | HCID 67212023 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | ethyl 3-amino-1H-pyrrolo[3,2-c]pyridine-2-carboxylate | HCID 23218185 | 55% |
Reaction Steps
To a solution of ethyl-4-(3-cyanopyridine)glycinate (2.47 g, 12.1 mmol) under nitrogen in EtOH (60 mL) was added sodium ethoxide (0.90 g, 13.3 mmol) and the mixture was heated at reflux for 1 hour. The mixture was allowed to cool to ambient temperature then quenched by the addition of water (3 mL) and saturated ammonium chloride solution (5 mL). The solvent was concentrated in vacuo, to provide a residue that was diluted with water (30 mL), and extracted with EtOAc (2×40 mL). The combined organic layers were dried (Na2SO4), filtered and evaporated to give the title compound as a brown solid (1.35 g, 55%). LCMS (method B): RT=0.61 min, M+H+=206.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07855216B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-45af08c7d9864d7e8e1a48054187e9c9 |
| Source note | uspto-grants-2010_12 |