Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 58292673 | HCID 58292673 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58292548 | HCID 58292548 | 15.7% |
Reaction Steps
1.25M HCl in methanol (5 mL, 6.0 mmol) was added to [6-(3-tert-butoxycarbonylamino-propoxy)-1-hydroxy-4-methyl-1,3-dihydro-benzo[c][1,2]oxaborol-3-yl]-acetic acid (0.345 g, 0.80 mmol) at room temperature and stirred for 18 hours then concentrated in vacuo. The residue was dissolved in THF (14 mL) and a solution of LiOH (0.229 g, 5.44 mmol) in water (5 mL) at 0° C. was added. The resulting mixture was stirred at room temperature for 3 hours then acidified to pH=2 with 6M HCl and extracted with EtOAc (3×25 mL). The organic extracts were washed with brine, dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by preparative HPLC to give [6-(3-amino-propoxy)-1-hydroxy-4-methyl-1,3-dihydro-benzo[c][1,2]oxaborol-3-yl]-acetic acid as a white solid (0.035 g, 14%). 1H NMR (400 MHz, methanol-d4) δ ppm 6.93 (br. s., 1H), 6.79 (br. s., 1H), 5.49 (d, J=5.86 Hz, 1H), 4.10 (t, J=5.47 Hz, 2H), 3.15 (t, J=7.03 Hz, 2H), 2.97 (d, J=14.85 Hz, 1H), 2.27 (s, 3H), 2.03-2.21 (m, 3H). MS (ESI) m/z: 280 [M+1]+. HPLC purity: 96.23% (Maxplot), 95.78% (220 nm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08343944B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-29d31052fc7a4d41b18549b8e30e5096 |
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| Source note | uspto-grants-2013_01 |
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