HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → HCID 58292552, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 58292664 | HCID 58292664 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58292552 | HCID 58292552 | 33.9% |
Reaction Steps
A solution of [6-(5-aminomethyl-pyrazin-2-yloxy)-1-hydroxy-4-methyl-1,3-dihydro-benzo[c][1,2]oxaborol-3-yl]-acetic acid ethyl ester (700 mg, 2.24 mmol) in THF (16 mL) was treated with LiOH (470 mg, 11.2 mmol) in water (8 mL) at room temperature for 2 h. The reaction was concentrated to dryness. The residue was diluted with water and adjusted to pH 3. The mixture was purified by preparative HPLC to give the title compound (250 mg). 1H NMR (300 MHz, CD3OD) δ 8.48 (s, 1H), 8.35 (s, 1H), 8.21 (s, 1H), 7.18 (s, 1H), 7.07 (s, 1H), 5.70-5.63 (m, 1H), 4.29 (s, 2H), 3.18-3.12 (m, 1H), 2.40 (s, 3H), 2.36-2.28 (m, 1H). MS found: (M+H)+=330.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08343944B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-7957550a480d41f4ab1ed21b6672c4ce |
| Source note | uspto-grants-2013_01 |