戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1663479作成日:2026年10月24日

Lawesson's reagent → 4-amino-N-(3-bromo-4-fluorophenyl)-1,2,5-thiadiazole-3-carbothioamide

https://huagongshe.com/ja/reaction/1663479

反応式

関与物質

役割名称HCID仕込み量
反応物Lawesson's reagentHCID 87949—
反応物4-amino-N-(3-bromo-4-fluorophenyl)-1,2,5-thiadiazole-3-carboxamideHCID 58558244—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物4-amino-N-(3-bromo-4-fluorophenyl)-1,2,5-thiadiazole-3-carbothioamideHCID 5855830955.7%

反応手順

A solution of 4-amino-N-(3-bromo-4-fluorophenyl)-1,2,5-thiadiazole-3-carboxamide (225 mg, 0.7 mmol) and 2,4-bis(4-methoxyphenyl)-2,4-dithioxo-1,3,2,4-dithiadiphosphetane (570 mg, 1.4 mmol) in toluene (6.8 mL) was stirred at 95° C. for 16 h. The reaction mixture was diluted with ethyl acetate (50 mL) and the insoluble salts were filtered. The filtrate was concentrated to a crude residue which was purified on silica gel to give the desired product (130 mg, 55%). LCMS for C9H7BrFN4S2 (M+H)+: m/z=332.8, 334.9.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08034953B2
出典データセットuspto-grants-2011_10
ORD IDord-c677cc94ebdf4e0b8ec7e081e68686cc
出典メモuspto-grants-2011_10