Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 86642694 | HCID 86642694 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86642693 | HCID 86642693 | 37.9% |
Reaction Steps
A mixture of chiral (S)-2-{[(2R,3S,4R,5S)-3-(3-chloro-2-fluoro-phenyl)-4-(4-chloro-2-fluoro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carbonyl]-amino}-3-thiazol-4-yl-propionic acid methyl ester trifluoroacetate salt (112 mg, 0.176 mmol) was dissolved in THF (3 mL) and methanol (1 mL), then 2N LiOH (1 mL) was added and stirred at room temperature for 2 hours. The mixture was diluted with water and extracted with ethyl acetate (2×), the organic phase was separated then concentrated under reduced pressure to afford the crude product that was purified by RP-HPLC (20-95% acetonitrile/water). The solvent was evaporated under reduced pressure to afford chiral (S)-2-{[(2R,3S,4R,5S)-3-(3-chloro-2-fluoro-phenyl)-4-(4-chloro-2-fluoro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carbonyl]-amino}-3-thiazol-4-yl-propionic acid trifluoroacetate salt as a white powder (41 mg, 37.9%). HRMS (ES+) m/z Calcd for C29H28Cl2F2N4O3S+H [(M+H)+]: 621.1300. found: 621.1298.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354444B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-4f1dd8a0b7a349979be2b4b5f23f2709 |
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| Source note | uspto-grants-2013_01 |
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