Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-(4-Chlorophenyl)-5-methyl-1,2-oxazole-4-carboxylic acid | HCID 1488093 | — |
| Product | HCID 24809797 | HCID 24809797 | 23.6% |
Reaction Steps
To 3-(4-chlorophenyl)-5-methylisoxazol-4-carboxylic acid (25 mg, 0.10 mmol) was added thionyl chloride (1 mL) and the neat solution allowed to stir 60° C. After 30 min, excess thionyl chloride was evaporated and dimethyl amine (40 μL, 0.08 mmol, 2 M in THF) was added and allowed to stir overnight at ambient temperature. The residue was purified using reversed phase HPLC to afford the title compound (5 mg). HRMS (ESI, pos. ion) m/z calcd for C13H13ClN2O2: 264.0666, found 264.0671.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07666888B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-0fd667abab7c4c9dab4639b08a3be5e4 |
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| Source note | uspto-grants-2010_02 |
|---|