Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 86690184 | HCID 86690184 | — |
| Reactant | 1419590-65-0 | HCID 131731278 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71227171 | HCID 71227171 | 62.6% |
Reaction Steps
2-Oxa-5-azaspiro[3.4]octane TFA salt (0.1.1 g, ca. 70%, 0.34 mmol) and 4-(1-(5-(4-(difluoromethyl)phenyl)-1,3,4-oxadiazole-2-carbonyl)azetidin-3-yloxy)-3-methoxybenzaldehyde (0.146 g, 0.34 mmol) were mixed in dichloromethane (2 ml). Triethylamine (0.1 ml, 0.72 mmol) was added, followed by sodium triacetoxyhydroborate (0.144 g, 0.68 mmol). The mixture was stirred at ambient temperature overnight (16 h). LC-MS showed some remaining starting material and an additional amount of sodium triacetoxyhydroborate (0.113 g) was added. Stirring continued for 6 h. The reaction mixture was then diluted with dichloromethane (10 ml) and shaken with NaHCO3 (sat. 3 ml). The two phases were separated by the use of a phase separator. Evaporation of the organic phase afforded a residue, which was purified by preparative reverse-phase HPLC at pH 10 to give 0.112 g (62%) of the desired product as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08685958B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-54a7929a10ea4dfbb9974f9fe7466191 |
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| Source note | uspto-grants-2014_04 |
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