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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPyridineHCID 1049—
ReactantSodium ThiosulfateHCID 24477—
ReactantBenzoylacetonitrileHCID 64799—
ReactantThioureaHCID 2723790—
SolventEthanolHCID 702—
Product2-Amino-4-Phenylthiazole-5-carbonitrileHCID 21455552—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993590B2
Source datasetuspto-grants-2015_03
ORD IDord-20d2e55bd4f34759bd8392d88d2dd222
Source noteuspto-grants-2015_03