HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[(2-Hydroxy-1,2-dimethylpropyl)amino]-7-(pyridin-3-ylethynyl)-5H-pyrido[4,3-b]indole-4-carboxamide → 1-[(2-Hydroxy-1,2-dimethylpropyl)amino]-7-(2-pyridin-3-ylethyl)-5H-pyrido[4,3-b]indole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[(2-Hydroxy-1,2-dimethylpropyl)amino]-7-(pyridin-3-ylethynyl)-5H-pyrido[4,3-b]indole-4-carboxamide | HCID 59543163 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[(2-Hydroxy-1,2-dimethylpropyl)amino]-7-(2-pyridin-3-ylethyl)-5H-pyrido[4,3-b]indole-4-carboxamide | HCID 42636046 | — |
Reaction Steps
Hydrogen was bubbled through a solution of 1-[(2-hydroxy-1,2-dimethylpropyl)amino]-7-(pyridin-3-ylethynyl)-5H-pyrido[4,3-b]indole-4-carboxamide (10 mg, 0.024 mmol) and Pd/C (10%, 2.6 mg) in EtOH (1.3 mL). After complete conversion, the mixture was purged with nitrogen, filtered through a pad of Celite, and concentrate to afford the title compound. LRMS (APCI) calc'd for (C24H27N5O2) [M+H]+, 418.2. found 418.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431569B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-f261eab483834958bc6a3db1a4d739c9 |
| Source note | uspto-grants-2013_04 |