HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-benzyloxycarbonyl-3-(R)-[1-[N-(tert-butoxycarbonyl)-N-(methyl)Amino]Cyclopropyl]Pyrrolidine → tert-Butyl methyl{1-[(3R)-pyrrolidin-3-yl]cyclopropyl}carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-benzyloxycarbonyl-3-(R)-[1-[N-(tert-butoxycarbonyl)-N-(methyl)Amino]Cyclopropyl]Pyrrolidine | HCID 22940376 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl methyl{1-[(3R)-pyrrolidin-3-yl]cyclopropyl}carbamate | HCID 67271848 | — |
Reaction Steps
1-benzyloxycarbonyl-3-(R)-[1-[N-(tert-butoxycarbonyl)-N-(methyl)amino]cyclopropyl]pyrrolidine (1.31 g, 3.48 mmol) was dissolved in ethanol (13 ml), and after adding a 10% palladium carbon catalyst (water content: 50%; 0.65 g) thereto, it was stirred at room temperature for 5 hours under a hydrogen atmosphere at atmospheric pressure. After performing filtration through cellite (ethanol washing), the filtrate was concentrated under a reduced pressure. As a result, 0.92 g (quantitative) of the title compound was obtained in the form of a colorless syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902226B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-cd6272a50cb147ce8868c78872da3d37 |
| Source note | uspto-grants-2011_03 |