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HRID 427485作成日:2026年10月26日

Methylamine → 8-(2-ethyl-6-methylbenzylamino)-N, 2,3-trimethylimidazo[1,2-a]pyridine-6-carboxamide

https://huagongshe.com/reaction/427485

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
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8-(2-ethyl-6-methylbenzylamino)-N, 2,3-trimethylimidazo[1,2-a]pyridine-6-carboxamideHCID 986324226%

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) and the reaction mixture was stirred at room temperature for 15 min. Methylamine (0.1 g, 3.2 mmol) was added and the reaction mixture was stirred at ambient temperature for 1.5 h. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography on silica gel using ethylacetate:methylene chloride (1:1) as eluent. The yield was treated with diethyl ether to give 40 mg (26%) of the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313137B1
出典データセットuspto-grants-2001_11
ORD IDord-21e4605fc6fd4ff89efa148354f82356
出典メモuspto-grants-2001_11