Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 68443873 | HCID 68443873 | — |
| Reactant | HCID 86633026 | HCID 86633026 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 24871998 | HCID 24871998 | 83.1% |
Reaction Steps
A solution of N-(5-(ethoxymethyl)-2-methylphenyl)ethanamide (344 mg, 1.66 mmol) in DMF (5 mL) was added to a suspension of NaH (133 mg, 3.32 mmol, 60% dispersion in mineral oil) in DMF (5 mL) at 0° C. under an atmosphere of argon. The mixture was stirred for 1 h at room temperature and cooled to 0° C. A solution of 2-chloro-5-(2-chloropyridin-4-yl)oxazole (357 mg, 1.66 mmol) in DMF (5 mL) was added dropwise to the mixture. After 1 h at 0° C., the reaction was poured into ice water (20 mL) and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4) and filtered. After removal of solvent the residue was silica gel column chromatographed (CH2Cl2/Ethanol:98/2) to give 474 mg of 5-(2-chloropyridin-4-yl)-N-(5-(ethoxymethyl)-2-methylphenyl) oxazol-2-amine (83%) as a beige solide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08080669B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-6dbe2aa358f64272bc476f941d8aed7b |
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| Source note | uspto-grants-2011_12 |
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