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HRID 31417作成日:2026年10月26日

Thiophene-3-carboxylic acid → N-(3-Iodo-4-methylphenyl)thiophene-3-carboxamide

https://huagongshe.com/reaction/31417

反応式

関与物質

役割名称HCID仕込み量
反応物Thiophene-3-carboxylic acidHCID 6918—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物DiisopropylethylamineHCID 81531—
反応物3-Iodo-p-toluidineHCID 118889—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
溶媒DimethylformamideHCID 6228—
生成物N-(3-Iodo-4-methylphenyl)thiophene-3-carboxamideHCID 21914512—

反応手順

Thiophene-3-carboxylic acid (2.75 g, 21.45 mmol) and HATU (8.15 g, 21.45 mmol) in DMF (25 ml) were stirred at room temperature for 15 mins. HOBT (2.9 g, 21.45 mmol), 3-iodo-4-methylaniline (5.0 g, 21.45 mmol) and DIPEA (11.2 ml, 64.35 mmol) were added and the reaction stirred at room temperature for 16 hrs. The solvent was evaporated under vacuum and the residue partitioned between ethyl acetate (100 ml) and aqueous sodium carbonate (10%, 100 ml). The aqueous layer was extracted with ethyl acetate (50 ml) and the combined organic phases washed with hydrochloric acid (2N, 75 ml), water (75 ml) and brine (75 ml). The organic phase was dried (magnesium sulphate) and absorbed onto silica. The silica was applied to a flash silica column and eluted with cyclohexane/ethyl acetate (4:1). The solvent was evaporated from the product fractions under vacuum to give N-(3-iodo-4-methylphenyl)thiophene-3-amide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425555B2
出典データセットuspto-grants-2008_09
ORD IDord-0bd633060a584cd0a32879a455ea2311
出典メモuspto-grants-2008_09