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HRID 1088292作成日:2026年10月27日

Flufenamic Acid → 2-[(3-Trifluoromethylphenyl)amino]-benzoic acid, 2-(aminothioxomethyl)hydrazide

https://huagongshe.com/reaction/1088292

反応式

関与物質

役割名称HCID仕込み量
反応物Flufenamic AcidHCID 3371—
反応物ThiosemicarbazideHCID 2723789—
溶媒PyridineHCID 1049—
溶媒TetrahydrofuranHCID 8028—
生成物2-[(3-Trifluoromethylphenyl)amino]-benzoic acid, 2-(aminothioxomethyl)hydrazideHCID 1567860444%

反応手順

N,N'-Carbonyldiimidazole (4.56 g, 27.6 mmol) is added to a room temperature solution of flufenamic acid (5.07 g, 18.0 mmol) in 70 ml of tetrahydrofuran. The clear yellow solution is stirred at room temperature for three hours. The solution is then added via cannula to a suspension of thiosemicarbazide (3.41 g, 37.5 mmol) in 55 ml of pyridine. The suspension is heated at reflux overnight. The clear orange solution is concentrated in vacuo and the residue is partitioned between ethyl acetate and water. The organic layer is washed with water, dried over magnesium sulfate and concentrated. The resulting solid is slurried with a 1:3 mixture of ethyl acetate and hexane. The off-white solid is collected by filtration providing 2.80 g (44%) of 2-[(3-trifluoromethylphenyl)amino]-benzoic acid, 2-(aminothioxomethyl)hydrazide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04962119
出典データセットuspto-grants-1990_10
ORD IDord-84610cee270b43a19bc9ce033ecb0aa3
出典メモuspto-grants-1990_10