Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66668306 | HCID 66668306 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66668795 | HCID 66668795 | — |
Reaction Steps
To a solution of (5-{4-[(−)-3-(2-methyl-pyridin-4-yl)-3-oxo-1-o-tolyl-propyl]-phenyl}-[1,3,4]oxadiazol-2-yl)-acetic acid ethyl ester (146 mg) in a mixture of ethanol (5 mL) and water (1.25 mL) was added sodium hydrogencarbonate (104 mg) and the reaction mixture stirred at room temperature for 4 h. The solution was adjusted to approximately pH 3 by using 1 M aqueous hydrochloric acid and then extracted over a sat. solution of brine (50 mL) with ethyl acetate (3×50 mL). The combined organic phases were dried over sodium sulfate and the crude reaction product purified by silica gel chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of dichloromethane:methanol (100:0 to 90:10). Light yellow solid. MS (ESI+): m/z=442.4 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08765730B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-74ff5db7545d4088afff109e4d00eb4e |
|---|
| Source note | uspto-grants-2014_07 |
|---|