HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → Ethyl glycyl-3-(6-methoxy-2-pyridinyl)alaninate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | ethyl N-(tert-butoxycarbonyl)glycyl-3-(6-methoxy-2-pyridinyl)alaninate | HCID 66582662 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl glycyl-3-(6-methoxy-2-pyridinyl)alaninate | HCID 66582543 | — |
Reaction Steps
To a 100-mL round-bottomed flask was added ethyl N-(tert-butoxycarbonyl)glycyl-3-(6-methoxy-2-pyridinyl)alaninate (1.28 g, 3.36 mmol) and trifluoroacetic acid (5 mL, 67.3 mmol) in DCM (5 mL). The reaction mixture was stirred at room temperature for 3 h. The solvent was removed in vacuo to give the crude ethyl glycyl-3-(6-methoxy-2-pyridinyl)alaninate as a colorless viscous oil, which was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431563B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-958deafd10b74a7e96a51cd647bb0dff |
| Source note | uspto-grants-2013_04 |