HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178418361, compound → HCID 178515172, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178515173 | HCID 178515173 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178515172 | HCID 178515172 | — |
Reaction Steps
22 g. of 6-chloropyrazolo[1,5-a]pyrido[4,3-d]pyrimidin-9(4H)-one of Example 1 are hydrogenated in 200 ml. of dimethylformamide in the presence of 15 g. of triethylamine and 10% palladium on charcoal as catalyst at 80° and 3 atmospheres hydrogen pressure. When the theoretical amount of hydrogen has been absorbed, the reaction is stopped and the mixture is filtered after cooling to room temperature. After evaporation of the solvent, the crystalline residue, pyrazolo[1,5-a]pyrido[4,3-d]pyrimidin-9(4H)-one, is recrystallized from dimethylformamide, yield: 13 g. (70%); m.p. >300°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075210 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-cde2fdf2632e4663af86616d5985c726 |
| Source note | uspto-grants-1978_02 |