HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20141227, compound → HCID 20141228, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20141227 | HCID 20141227 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20141228 | HCID 20141228 | 67% |
Reaction Steps
Dissolved in 10 ml of ethanol was 0.2 g (0.55 mmol) of 6,9-dimethyl-2-(4-benzylpiperazino)-5-oxo-5,6,7,8-tetrahydro(9H)pyrimido[4,5-e]diazepine, followed by an addition of 20 mg of 10% Pd-C. Under reflux, the reactant was hydrogenated at atmospheric pressure for 2 hours. After cooling the reaction mixture to room temperature, the catalyst was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography to obtain 0.1 g of the intended product (yield: 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04734418 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-5365d6dbfe0746579f51d7f8c6ef2ed4 |
| Source note | uspto-grants-1988_03 |