Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13784145 | HCID 13784145 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13784146 | HCID 13784146 | 96.7% |
Reaction Steps
Added to 30 ml of THF were 0.65 g (1.84 mmol, Referential Example 51) of 2-(4-benzylpiperazino)-6-oxo-6,7,8,9-tetrahydro(5H)pyrimido[5,4-b]azepine and 0.15 g (3.75 mmol) of 60% NaH. The resultant mixture was stirred at 20° C. for 30 minutes. Thereafter, 3 g (27.8 mmol) of ethyl bromide was added and the reaction mixture was heated to 60° C. at which the reaction was conducted for 5 hours. After completion of the reaction, the solvent was distilled off and the residue was purified by silica gel column chromatography to obtain 0.65 g of a colorless oil (yield: 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04734418 |
|---|
| Source dataset | uspto-grants-1988_03 |
|---|
| ORD ID | ord-1d7711ee40d045a597ef5c7fabbd7579 |
|---|
| Source note | uspto-grants-1988_03 |
|---|