HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 71227163, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 58043115 | HCID 58043115 | — |
| Reactant | 5-Oxa-2-azaspiro[3.4]octane hydrochloride | HCID 86280355 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71227163 | HCID 71227163 | 98.5% |
Reaction Steps
To a solution of 4-(1-(5-phenyl-1,3,4-oxadiazole-2-carbonyl)azetidin-3-yloxy)benzaldehyde (70 mg, 0.20 mmol) in dichloromethane (2 mL) was added 5-oxa-2-azaspiro[3.4]octane hydrochloride (80 mg, 0.53 mmol) and triethylamine (0.100 mL, 0.72 mmol). After stirring at ambient temperature for 30 minutes, sodium triacetoxyhydroborate (70 mg, 0.33 mmol) was added. Stirring was continued at ambient temperature overnight, after which NaHCO3 (aq, sat, 5 ml) was added. The phases were separated with the aid of a phase separator. The aqueous phase was extracted twice with dichloromethane and dried with the aid of a phase separator. The combined organic phases were concentrated in vacuo to afford 88 mg of a colourless residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08685958B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-29159a8b01e64ee6a1cabda757346737 |
| Source note | uspto-grants-2014_04 |