HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(5-Furan-3-yl-4-phenyl-thiazol-2-yl)-formamide → 5-Furan-3-yl-4-phenyl-thiazol-2-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(5-Furan-3-yl-4-phenyl-thiazol-2-yl)-formamide | HCID 57709597 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Furan-3-yl-4-phenyl-thiazol-2-ylamine | HCID 57709610 | — |
Reaction Steps
N-(5-Furan-3-yl-4-phenyl-thiazol-2-yl)-formamide (5.7 g, 21 mmol) was dissolved in a mixture of methanol (210 mL) and THF (90 mL), and conc. squeous hydrochloric acid (8.7 mL) was added dropwise at room temperature. The reaction mixture was stirred over night and the solvent was removed by evaporation. The residue was extracted with ethyl acetate, and washed with NaHCO3 (aq.; sat.) and water and dried over sodium sulfate. The solvent was removed and the crude product was purified on neutral Al2O3 using 30-35% ethyl acetate in hexane as eluent. Yield: 2.5 g, 49%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910613B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-6890e186cbf1464eaad905c868b0c5c7 |
| Source note | uspto-grants-2011_03 |