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HRID 427475作成日:2026年10月26日

4-Ethoxyaniline → N-(4-ethoxyphenyl)-8-(2-ethyl-6-methylbenzylamino)-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxamide

https://huagongshe.com/reaction/427475

反応式

関与物質

役割名称HCID仕込み量
反応物4-EthoxyanilineHCID 9076—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物2,3-Dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo[1,2-a]pyridine-6-carboxylic acidHCID 11823936—
溶媒DichloromethaneHCID 6344—
生成物N-(4-ethoxyphenyl)-8-(2-ethyl-6-methylbenzylamino)-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxamideHCID 989029674%

反応手順

2,3-Dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo[1,2-a]pyridine-6-carboxylic acid (0.15 g, 0.44 mmol) and o-Benzotriazol-1-yl-N,N,N′,N′-Tetramethyluronium tetrafluoroborate (TBTU)(0.14 g, 0.44 mmol) were added to methylene chloride (10 ml). 4-ethoxyanilin(0.19 g, 1.4 mmol) was added and the reaction mixture was stirred at ambient temperature for 72 h. The solvent was evaporated under reduced pressure and the residue was added to a column with silica gel and was purified by chromatography using methylene chloride:methanol (95:5) as eluent. The residue was treated with a hot mixture of hexane:ethyl acetate (2:1) and the product was filtered off and dried to obtain 0.14 g (74%) of the desired compound as white crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313136B1
出典データセットuspto-grants-2001_11
ORD IDord-a123a0544214479c886360d44421ef5a
出典メモuspto-grants-2001_11