HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 9-[(Phenyl)methyl]-2-methyl-4-hydroxy-5-carbamoyl carbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 9-[(Phenyl)methyl]-2-methyl-4-hydroxy-5-carbomethoxy carbazole | HCID 22739752 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 9-[(Phenyl)methyl]-2-methyl-4-hydroxy-5-carbamoyl carbazole | HCID 22739371 | 44% |
Reaction Steps
A solution of the 9-[(phenyl)methyl]-2-methyl-4-hydroxy-5-carbomethoxy carbazole (470 mg, 1.36 mM) in 20 ml THF and 80 mL concentrated aqueous ammonium hydroxide was sonicated for 6 hours at 30-40° C. The precipitated solid was filtered and triturated with Et2O to afford 200 mg (44%) of 9-[(phenyl)methyl]-2-methyl-4-hydroxy-5-carbamoyl carbazole. 1H NMR (DMSO-d6) δ 10.5 (s, 1H), 8.8 (bs, 1H), 8.4 (bs, 1H), 7.75 (m, 1H), 7.4 (m, 2H), 7.25 (m, 3H), 7.1 (m, 2H), 6.95 (s, 1H), 6.45 (s, 1H), 5.65 (s, 2H), 2.4 (s, 3H). MS (ES) m/e 314, 331.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06177440B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-9e1ba368089a465a9c3f3424ac1de67d |
| Source note | uspto-grants-2001_01 |