Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | p-Fluorobenzoylacetonitrile | HCID 2783172 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 83535263 | HCID 83535263 | — |
Reaction Steps
To a solution of 4-fluorobenzoylacetonitrile (50 g, 306 mmol, 1 eq.) in EtOH (600 mL) was added pyridine (24.7 mL, 306 mmol, 1 eq.). The resulting mixture was stirred at 70° C. for 15 min then cooled to r.t. A previously stirred suspension of thiourea (46.7 g, 613 mmol, 2 eq.) and iodine (77.8 g, 306 mmol, 1 eq.) in EtOH (300 mL) was then slowly added. After 1 h at r.t. a cold 1 M Na2S2O3 solution (360 mL) was added under stirring. The resulting precipitate was filtered, washed with water, and finally dried under vacuo to afford 2-Amino-4-(4-fluoro-phenyl)-thiazole-5-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993590B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-fd0776f05a314625929195c8ff0adb2d |
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| Source note | uspto-grants-2015_03 |
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