HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13784145, compound → HCID 13784148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13784145 | HCID 13784145 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13784148 | HCID 13784148 | 99.7% |
Reaction Steps
Added to 20 ml of ethanol were 0.1 g (0.3 mmol, Referential Example 51) of 2-(4-benzylpiperazino)-6-oxo-6,7,8,9-tetrahydro(5H)pyrimido[5,4-b]azepine and 0.01 g of 10% Pd-C. In a hydrogen atmosphere, they were reacted at 50° C. for 4 hours. After filtering off the Pd-C, the filtrate was dried to solid to obtain 0.074 g of colorless crystals in a quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04734418 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-2a475a732bf34714ad6ddc99372d86b4 |
| Source note | uspto-grants-1988_03 |