Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 58292578 | HCID 58292578 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58292575 | HCID 58292575 | 18.2% |
Reaction Steps
To a solution of ethyl 2-(1,4-dihydroxy-6-(pyrazin-2-yloxy)-1,3-dihydrobenzo[c][1,2]oxaborol-3-yl)acetate (100 mg, 0.31 mmol) in EtOH (5 ml) was added an aqueous solution of lithium hydroxide (26.1 mg, 0.62 mmol) in water (1 mL). The reaction mixture was stirred at room temperature overnight and acidified with 1 N HCl to pH=3. The resulting mixture was extracted with EtOAc (20 mL) and combined organic layers were washed with water (15 mL) and brine (15 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by prep HPLC to give the title compound as a white powder (17 mg, yield: 18%). 1H NMR (400 MHz, DMSO-d6) δ 12.31 (s, 1H), 10.13 (s, 1H), 9.19 (s, 1H), 8.54 (s, 1H), 8.38 (d, J=2.8 Hz, 1H), 8.24 (d, J=1.2 Hz, 1H), 6.90 (d, J=1.6 Hz, 1H), 5.44 (m, 1H), 3.22 (m, 1H), 2.18-2.11 (m, 1H). MS (ESI) m/z=303 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08343944B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-b71e425868d745b78163692b437493e3 |
|---|
| Source note | uspto-grants-2013_01 |
|---|