Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 6-chloropyridine-3-carboxylate | HCID 254249 | — |
| Reactant | 3-Hydroxy-5-[(propan-2-yl)oxy]-N-(1,3-thiazol-2-yl)benzamide | HCID 23093039 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10431879 | HCID 10431879 | — |
Reaction Steps
After adding 123 mg (0.72 mmol) of 6-chloronicotinic acid methyl ester and 199 mg (1.44 mmol) of potassium carbonate to a solution of 100 mg (0.36 mmol) of the obtained amide compound in N,N-dimethylfommamide (10.0 ml), the mixture was stirred at 80° C. for 18 hours under a nitrogen atmosphere. Water was added to the reaction mixture, extraction was performed with ethyl acetate, and the organic layer was dried and then concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (hexane:ethyl acetate=3:1) to obtain the title compound as a white solid. The analysis data for the compound obtained in Production Example 65 are shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754743B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-f9583c8db9a1475abb7430f6e7f34243 |
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| Source note | uspto-grants-2010_07 |
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