HuagongsheHuagongshe Chemistry Print Report · For research reference only
7H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamide → 5H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamide | HCID 68846942 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamide | HCID 68849291 | — |
Reaction Steps
10% Palladium on carbon (70 mg, 0.07 mmol) was added to a solution of 7H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamide, 13-cyclohexyl-N10-[(dimethylamino)sulfonyl]-N6-(2-hydroxyethyl)-3-methoxy-N6-methyl- (64 mg, 0.11 mmol) in MeOH (3 mL) and the reaction mixture was vacuum flushed with nitrogen (3×) and then with hydrogen (3×). The reaction was stirred under a balloon of hydrogen overnight, filtered through a pad of celite and concentrated to yield 5H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamide, 13-cyclohexyl-N10-[(dimethylamino)sulfonyl]-6,7-dihydro-N6-(2-hydroxyethyl)-3-methoxy-N6-methyl-(50 mg, 0.08 mmol, 78%) as a yellow solid. Mixture of atrope diasteromers:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07348425B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-31163c0607e44434b0babd5b1c9f6394 |
| Source note | uspto-grants-2008_03 |