HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium ethoxide → 7-bromo-2-chloro-4-ethoxy-5H-pyrimido[5,4-b]indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 7-bromo-2,4-dichloro-5H-pyrimido[5,4-b]indole | HCID 58118487 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-bromo-2-chloro-4-ethoxy-5H-pyrimido[5,4-b]indole | HCID 58118536 | 99% |
Reaction Steps
5 g (15.8 mmol) 7-bromo-2,4-dichloro-5H-pyrimido[5,4-b]indole was suspended in 20 ml ethanol and mixed with 15.8 ml (31.5 mmol) 2M sodium ethylate solution (EtOH). The mixture was refluxed for 9.5 h. Having cooled down to room temperature, the solvent was concentrated and water was added. The resulting precipitate was sucked off and washed with water. 5.1 g (99%) 7-bromo-2-chloro-4-ethoxy-5H-pyrimido[5,4-b]indole was obtained. ESI-MS [m/z]: 324, 326 [M−H]−
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08664233B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-144a92e9a70c48b78e46818f1b0da403 |
| Source note | uspto-grants-2014_03 |