Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 57473613 | HCID 57473613 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57473614 | HCID 57473614 | 95% |
Reaction Steps
To an ambient temperature solution of 3-(1-{4-[2-(2,6-Dichloro-phenyl)-4-isopropyl-2H-pyrazol-3-ylmethoxy]-2-methyl-phenyl}-1-methyl-ethylsulfanyl)-benzoic acid methyl ester (91 mg, 0.156 mmol) in dioxane (2 mL) is added a solution of lithium hydroxide (234 μL, 0.468 mmol, 2.0N in water). The reaction mixture is heated to 50° C. The reaction mixture is concentrated and the residue is partitioned between Et2O and water. The aqueous layer pH is adjusted to approximately 4 and is extracted with a second portion of Et2O. The combined organic layers are washed with water, dried (MgSO4), filtered, and concentrated to yield the title compound (84 mg, 95%). ES/MS m/e (35Cl) 569.0 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846960B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-88d3136b8bcf40bc883f406f72e57b4f |
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| Source note | uspto-grants-2010_12 |
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