HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylmethyl 4-((6,7-dihydro[1,4]dioxino[2,3-c]pyridazin-3-ylmethyl){[(1,1-dimethylethyl)oxy]carbonyl}amino)-1-piperidinecarboxylate → 1,1-Dimethylethyl (6,7-dihydro[1,4]dioxino[2,3-c]pyridazin-3-ylmethyl)4-piperidinylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylmethyl 4-((6,7-dihydro[1,4]dioxino[2,3-c]pyridazin-3-ylmethyl){[(1,1-dimethylethyl)oxy]carbonyl}amino)-1-piperidinecarboxylate | HCID 68992990 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,1-Dimethylethyl (6,7-dihydro[1,4]dioxino[2,3-c]pyridazin-3-ylmethyl)4-piperidinylcarbamate | HCID 86635330 | 97% |
Reaction Steps
Phenylmethyl 4-((6,7-dihydro[1,4]dioxino[2,3-c]pyridazin-3-ylmethyl) {[(1,1-dimethylethyl)oxy]carbonyl}amino)-1-piperidinecarboxylate (11.89 g. 25 mmol) in ethanol (90 ml) was hydrogenated with 10% palladium on charcoal (aqueous paste, 2 g) for 21 h. The mixture was filtered and evaporated to give a white solid (8.5 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071592B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-8c54f8abe94546d5bf09cc9faea1329f |
| Source note | uspto-grants-2011_12 |