HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880602Generated: November 3, 2026
Iodine → 2-Amino-4-Phenylthiazole-5-carbonitrile
https://huagongshe.com/reaction/880602
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Benzoylacetonitrile | HCID 64799 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Amino-4-Phenylthiazole-5-carbonitrile | HCID 21455552 | — |
Reaction Steps
To a solution of benzoylacetonitrile derivative (1 eq.) in EtOH is added pyridine (1 eq.). The resulting mixture is stirred at 70° C. for 15 min then cooled at r.t. A previously stirred suspension of thiourea (2 eq.) and iodine (1 eq.) in EtOH is then slowly added. After 1 h at r.t. a cold 1M Na2S2O3 solution is added under stirring. The resulting precipitate is filtered, washed with water, and finally dried under vacuo to afford the amino-4-phenyl-thiazole-5-carbonitrile derivative.
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-20d2e55bd4f34759bd8392d88d2dd222 |
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| Source note | uspto-grants-2015_03 |
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