HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 71115295, compound → Methyl (S)-3-tert-butoxycarbonylamino-2-piperazin-1-ylpropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 71115295 | HCID 71115295 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl (S)-3-tert-butoxycarbonylamino-2-piperazin-1-ylpropanoate | HCID 86675027 | — |
Reaction Steps
(21 mmol) of methyl(S)-2-(4-benzylpiperazin-1-yl)-3-tert-butoxycarbonylaminopropanoate (prepared as described in example 17.4) in 120 ml of ethanol, degassed beforehand under a nitrogen stream. The reaction medium is then placed under a hydrogen atmospheric pressure for 24 h and then filtered through celite and thoroughly rinsed with dichloromethane. After concentration under vacuum, 6.1 g (100%) of methyl (S)-3-tert-butoxycarbonylamino-2-piperazin-1-ylpropanoate are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633196B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-98521336825a40faa03a61adc1650cd6 |
| Source note | uspto-grants-2014_01 |