Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 59208496 | HCID 59208496 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59208514 | HCID 59208514 | 84.3% |
Reaction Steps
To a stirred solution of ethyl 2-[6-(3-ethyl-ureido)-pyridin-3-yl]-4-propylcarbamoyl-thiazole-5-carboxylate (Example 62, 0.33 g, 0.8 mM) in methanol (15 mL) was added 2 N lithium hydroxide (4 mL). The mixture was heated to 50° C. overnight, then concentrated to dryness. 2N hydrochloric acid was added to the concentrate, and the precipitated solid was filtered and dried under vacuum to afford 0.259 g (72%) of the title compound as solid. NMR: 0.92 (t, 3H), 1.10 (t, 3H), 1.63 (m, 2H), 3.20 (q, 2H), 3.36 (q, 2H), 7.67 (d, 1H), 7.68 (br s, 1H), 8.39 (dd, 1H), 9.02 (s, 1H), 9.62 (br s, 1H), 9.78 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674801B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-4b79de66fda246ce875d0b38a26b13ca |
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| Source note | uspto-grants-2010_03 |
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