HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → HCID 66604487, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 66605755 | HCID 66605755 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66604487 | HCID 66604487 | 93% |
Reaction Steps
A mixture of benzyl 8-carbamoyl-6-(3-methoxyphenyl)-9H-carbazol-2-ylcarbamate (95 mg, 0.204 mmol, Example 136), palladium on carbon (10%) (39.5 mg, 0.037 mmol) and ammonium formate (77 mg, 1.224 mmol) in MeOH (5 mL) was flushed with nitrogen and heated at reflux for 1 hr. The reaction mixture was cooled to room temperature and filtered. The solvent was removed from the filtrate to leave 7-amino-3-(3-methoxyphenyl)-9H-carbazole-1-carboxamide (68 mg, 0.189 mmol, 93% yield) as a solid. MS (ESI) m/z 332.1 (M+H). 1H NMR (MeOD) δ ppm 8.31 (1H, d, J=1.53 Hz), 8.02 (1H, d, J=1.53 Hz), 7.89 (1H, d, J=8.24 Hz), 7.26 -7.47 (3H, m), 6.83-7.01 (2H, m), 6.71 (1H, dd, J=8.24, 1.83 Hz), 3.91 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08815840B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-36bbc61cf7334334a312f8e47357160b |
| Source note | uspto-grants-2014_08 |