Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Chloromethyl isopropyl carbonate | HCID 14787051 | — |
| Reactant | HCID 178521475 | HCID 178521475 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Product | HCID 86705126 | HCID 86705126 | 19.1% |
Reaction Steps
A mixture of chloromethyl isopropyl carbonate (15.6 mg, 102 μmol) and NaI (15.3 mg, 102 μmol) in acetone (0.7 mL, 10 mmol) was stirred at 65° C. for 1 hour, then added (R)-3-[N-(3′-chlorobiphenyl-4-ylmethyl)-N′-(3-hydroxyisoxazole-5-carbonyl)hydrazino]-2-hydroxypropionic acid 2-oxo-2-phenylethyl ester (20.0 mg, 36.4 μmol) that had been dissolved in acetone (0.4 mL, 5 mmol) at room temperature and treated with cesium carbonate (13.0 mg, 40 μmol). The resulting mixture was then heated at 40° C. for 1 hour. DIPEA (0.2 mL, 1 mmol) was added and heating continued for 1 hour. The mixture was cooled to room temperature and concentrated. The residue was partitioned between EtOAc (10.0 mL) and water (2.0 mL). The organic layer was washed with saturated aqueous NaHCO3 (3.0 mL), saturated aqueous NaCl (3.0 mL), dried over Na2SO4, filtered, and concentrated. Zinc 90.8 mg, 1.4 mmol) and AcOH (0.5 mL, 9 mmol) were added and the resulting mixture was stirred at room temperature for 1 hour. The solids were washed with AcOH (1.0 mL) then filtered. The filtrates were combined and purified by reverse phase preparative HPLC to yield the title compound (3.8 mg). MS m/z [M+H]+ calc'd for C25H26ClN3O9, 548.14. found 548.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871792B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-97e85896bde443e6bf2fd339dc4d96f3 |
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| Source note | uspto-grants-2014_10 |
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