Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Chloro-3-(1-cyano-1-methylethyl)benzoic acid | HCID 66810425 | — |
| Reactant | HCID 86646025 | HCID 86646025 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Solvent | Oxalyl chloride | HCID 65578 | — |
| Product | HCID 59507054 | HCID 59507054 | 21.4% |
Reaction Steps
To a solution of 4-chloro-3-(1-cyano-1-methylethyl)benzoic acid (0.11 g, 0.5 mmol) in oxalyl chloride (0.5 mL) was added N,N-dimethylformamide (40 μL), and the mixture was stirred at room temperature for 30 min, and concentrated to dryness under reduced pressure. This was dissolved in a mixture of N,N-dimethylacetamide (1 mL) and tetrahydrofuran (1 mL), and a solution was added dropwise to a solution of N-[5-(3-amino-4-fluorophenoxy)[1,3]thiazolo[5,4-b]pyridin-2-yl]acetamide (0.11 g, 0.33 mmol) produced in Example C64(ii) in N,N-dimethylacetamide (1 mL) under ice-cooling. The reaction mixture was stirred at room temperature for 3 hr, and poured into water (100 mL), and the mixture was extracted with ethyl acetate (100 mL×2). The ethyl acetate layers were combined, and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/hexane=0/100→100/0), and recrystallized from methanol to give the title compound (37 mg, 21%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344135B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-56efdf31decf4c6996136933d4097eb5 |
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| Source note | uspto-grants-2013_01 |
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