Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 58119308 | HCID 58119308 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 44815805 | HCID 44815805 | 37% |
Reaction Steps
To 3-(4-{5-[(4-chlorophenyl)thio]-2-phenyl-1,3oxazol-4-yl}benzonitrile (30 mg, 0.075 mmol) in 2 mL EtOH was added 0.25 mL of 50% aqueous NH2OH and catalytic amount of K2CO3. The reaction was heated at 120° C. for 1 h via microwave irradiation. The reaction mixture was concentrated to dryness and the residue was dissolved in 5 mL triethylorthoformate. A catalytic amount of TFA was added, and the reaction was heated at 130° C. for 3 h. The volatiles were removed and the residue was purified by reverse phase HPLC to afford 12 mg (37% yield) of the title compound: m/z 432.1 (M+H)+. 1H NMR (500 MHz, CDCl3: 8.8 (1H, s), 8.39 (2H, d), 8.21 (2H, d), 8.19 (1H, m), 7.59 (4H, br), 7.24 (4H, br).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045467B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-9c2872fe85224562ad341b7edc07ced0 |
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| Source note | uspto-grants-2015_06 |
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