HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Azaindole → tert-Butyl N-(4-{1H-pyrrolo[2,3-c]pyridin-3-yl}cyclohex-3-en-1-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Azaindole | HCID 9219 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | tert-butyl N-(4-oxocyclohexyl)carbamate | HCID 1512535 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-Butyl N-(4-{1H-pyrrolo[2,3-c]pyridin-3-yl}cyclohex-3-en-1-yl)carbamate | HCID 68244193 | 78% |
Reaction Steps
A suspension of 1H-pyrrolo[2,3-c]pyridine (0.95 g, 8.05 mmol), tert-butyl (4-oxocyclohexyl)carbamate (1.82 g, 8.54 mmol) and KOH (0.95 g, 17.0 mmol) in MeOH (10 mL) was heated at reflux overnight. The solution was added to ice-water (50 mL) and then MeOH (50 mL) was added. The resulting solution was concentrated to circa 50 mL and extracted three times with DCM/MeOH (9:1, 50 mL) and the organic layers were combined and concentrated. The residue was purified by flash chromatography (9:1 DCM/MeOH) to give the title compound as a white solid (1.96 g, 78%). MS (ESI+) m/z=314 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09227967B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-1694d0eb951a4570abc05c7201d340d8 |
| Source note | uspto-grants-2016_01 |