Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 69299425 | HCID 69299425 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10323518 | HCID 10323518 | — |
Reaction Steps
(±)-3-(4-{2-Oxo-3-[4-(3-o-tolyl-ureido)phenyl]-2H-pyridin-1-ylmethyl}phenyl)-butyric acid methyl ester (0.21 g, 0.41 mmol) was dissolved in tetrahydrofuran (3 mL) and aqueous lithium hydroxide (0.5 M, 3 mL) added with stirring. The mixture was heated at 65° C. for 2 hours and then allowed to cool and concentrated in vacuo. The mixture was acidified with hydrochloric acid (2M), extracted with ethyl acetate (2×25 mL) and the combined organic layers washed with brine and dried over anhydrous magnesium sulfate. After filtration and evaporation to dryness the title compound was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07410984B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-66e56039b7bd48d9868c8e818d64222d |
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| Source note | uspto-grants-2008_08 |
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