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HRID 346491作成日:2026年10月26日

Sodium Iodide → 5-Chloro-3-[(phenylthio)methyl]-1,2,4-thiadiazole

https://huagongshe.com/reaction/346491

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物ThiophenolHCID 7969—
反応物Sodium CarbonateHCID 10340—
反応物5-Chloro-3-(chloromethyl)-1,2,4-thiadiazoleHCID 332610—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物5-Chloro-3-[(phenylthio)methyl]-1,2,4-thiadiazoleHCID 21081458—

反応手順

1.05 eq of NaI were dissolved in dry acetone. 1 eq of 5-chloro-3-(chloromethyl)-1,2,4-thiadiazole, 1.03 eq of the thiophenol and 1 eq of Na2CO3 were added and the reaction mixture was stirred at ambient temperature for 2 hours. The reaction mixture was diluted with EtOAc and water. The organic phase was washed with an aqueous solution of Na2SO3 (sat), dried over MgSO4 and evaporated in vacuo. Preparative HPLC purification gave the 5-chloro-3-[(phenylthio)methyl]-1,2,4-thiadiazole. This was subsequently dissolved in 95% ethanol and conc. NH3 (aq) was added. In some cases acetonitrile was added in order to completely dissolve the starting material. The mixture was transferred to a microwave tube and run in the microwave at 150° C. for 5 min. the reaction was quenched with water and the desired 3-arylthiomethyl-5-amino-1,2,4-thiadiazole worked up and purified using standard procedures.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07173030B2
出典データセットuspto-grants-2007_02
ORD IDord-111ed844a99d4345a191b2cd24b48c9b
出典メモuspto-grants-2007_02