Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | HCID 118157548 | HCID 118157548 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 90060382 | HCID 90060382 | 83.5% |
Reaction Steps
No. 5538573, (E)-(2S,3S)-12,12-difluoro-3-[(S)-2-(2′-fluoro-biphenyl-4-yl)-1-methoxycarbonyl-ethylcarbamoyl]-2-hydroxy-2-(2-methoxy-ethyl)-nonadec-4-enoic acid (8.2 mg, 0.0116 mmol) was dissolved in acetonitrile (0.328 mL), and water (0.0011 mL, 0.0611 mmol), triethylamine (0.0097 mL, 0.0696 mmol), and anhydrous lithium bromide (20.1 mg, 0.231 mmol) were then added at room temperature. The reaction mixture was stirred at 50° C. for 3.5 hours, cooled to room temperature, and then purified by preparative HPLC to obtain 6.7 mg of the title compound (0.00969 mmol, 83% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266853B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-c9a5c944820d4e03b2c473024d7cd0cb |
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| Source note | uspto-grants-2016_02 |
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