HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 8-oxa-1-azaspiro[4.5]decane-2-carboxylate → ethyl 1-{N-[(methyloxy)carbonyl]-L-valyl}-8-oxa-1-azaspiro[4.5]decane-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 8-oxa-1-azaspiro[4.5]decane-2-carboxylate | HCID 58313084 | — |
| Reactant | Carbamic acid, N-[(1S)-1-(chlorocarbonyl)-2-methylpropyl]-, methyl ester | HCID 86654825 | — |
| Catalyst | CID 101611454 | HCID 178509332 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 1-{N-[(methyloxy)carbonyl]-L-valyl}-8-oxa-1-azaspiro[4.5]decane-2-carboxylate | HCID 58313069 | 20% |
Reaction Steps
To a solution of ethyl 8-oxa-1-azaspiro[4.5]decane-2-carboxylate (166) (125 mg, 0.59 mmol) in anhydrous dichloromethane (2 mL) was added silver cyanide (98 mg, 0.73 mmol) followed by N-[(methyloxy)carbonyl]-L-valyl chloride (142 mg, 0.73 mmol) as a solution in anhydrous dichloromethane (3.5 mL) and the solution stirred at room temperature for 18 h under nitrogen. The reaction is filtered and treated with methanol and stirred for 5 minutes. The reaction is concentrated in vacuo and the residue purified by silica gel chromatography eluting with 30-100% hexanes/EtOAc to afford the title compound as a white solid (43 mg, 20% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150587B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-a1f8079401ca44db9163679a0404ec5a |
| Source note | uspto-grants-2015_10 |