HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Benzyloxycarbonyl-3-(4-methylpiperazin-1-yl)-carbonylmethoxy-4-methoxybenzylamine → 3-(4-Methylpiperazin-1-yl)-carbonylmethoxy-4-methoxybenzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Benzyloxycarbonyl-3-(4-methylpiperazin-1-yl)-carbonylmethoxy-4-methoxybenzylamine | HCID 54104530 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(4-Methylpiperazin-1-yl)-carbonylmethoxy-4-methoxybenzylamine | HCID 86754292 | 109.8% |
Reaction Steps
A mixture comprising 3.26 g of N-benzyloxycarbonyl-3-(4-methylpiperazin-1-yl)-carbonylmethoxy-4-methoxybenzylamine, 0.5 g of 5% palladium carbon and 70 ml of ethanol, was stirred at 60° C. for 6 hours in a hydrogen atmosphere and further at room temperature overnight. Palladium carbon was filtered off, and then the filtrate was distilled off under reduced pressure to obtain 2.45 g of the above-identified compound as slightly brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05929074 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-ba2ddf45bcba4d13af63ba1f59d1c124 |
| Source note | uspto-grants-1999_07 |