HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → HCID 58292762, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 58292740 | HCID 58292740 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 58292762 | HCID 58292762 | — |
Reaction Steps
To a solution of ethyl 2-(6-(2-aminopyridin-4-yloxy)-1-hydroxy-4-methyl-1,3-dihydrobenzo[c][1,2]oxaborol-3-yl)acetate in MeOH/THF (8 mL, 1:1) was added aqueous NaOH solution (200 mg in 2 mL of water). After stirring at room temperature for two hours, the reaction mixture was evaporated, acidified to pH 5 using 1 M HCl and then concentrated. HPLC purification gave desired product as a white powder. 1H NMR (400 MHz, DMSO-d6) δ 12.3 (b, 1H), 9.30 (b, 1H), 7.87 (d, J=7.2 Hz, 1H), 7.69 (b, 2H), 7.25 (d, J=2 Hz, 1H), 7.13 (d, J=2 Hz, 1H), 6.59 (dd, J=7.2, 2.8 Hz, 1H), 6.00 (d, J=2.4 Hz, 1H), 5.49 (dd, J=9.6, 2.4 Hz, 1H), 3.05 (dd, J=15.6, 2.4 Hz, 1H), 2.28 (s, 3H), 2.08 (dd, J=15.2, 9.6 Hz, 1H). MS (ESI) m/z=313 [M−H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08343944B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-c4272bb56f3e4a0e841ee680eabb9ae9 |
| Source note | uspto-grants-2013_01 |