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HRID 44334作成日:2026年10月24日

Benzoyl isothiocyanate → N-benzoyl-N'-(3-cyano-4,5-dimethyl-2-thienyl)thiourea

https://huagongshe.com/ja/reaction/44334

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl isothiocyanateHCID 68284—
反応物2-Amino-4,5-dimethyl-thiophene-3-carbonitrileHCID 290236—
溶媒1,4-DioxaneHCID 31275—
生成物N-benzoyl-N'-(3-cyano-4,5-dimethyl-2-thienyl)thioureaHCID 899430—

反応手順

To a solution of 2-amino-4,5-dimethylthiophene-3-carbonitrile (1.52 g, 10.0 mmol) in 1.4-dioxane (20 mL) was added benzoylisothiocyanate (1.63 g, 10.0 mmol). The reaction mixture was then stirred at room temperature under nitrogen overnight. The precipitation was collected by filtration, washed with EtOAc/Hexanes (1:4), and dried under vacuum overnight to give N-(3-Cyano-4,5-dimethylthiophen-2-ylcarbamothioyl)benzamide as a white solid. 1H NMR (400 MHz, CDCl3) δ2.23 (s, 3H), 2.31 (s, 3H), 7.58-7.54 (m, 2H), 7.68-7.66 (m, 1H), 7.94 (d, J=7.2 Hz, 2H), 9.13 (bs, 1H). MS 316 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541421B2
出典データセットuspto-grants-2013_09
ORD IDord-9f8d0ac715214716a431791d8beae02d
出典メモuspto-grants-2013_09