戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 427492作成日:2026年10月25日

Ethanolamine → 2,3 dimethyl-8-(2-ethyl-6-methylbenzylamino)-N-hydroxyethyl-imidazo[1,2-a]pyridine-6-carboxamide

https://huagongshe.com/reaction/427492

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolamineHCID 700—
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2,3 dimethyl-8-(2-ethyl-6-methylbenzylamino)-N-hydroxyethyl-imidazo[1,2-a]pyridine-6-carboxamideHCID 9821241—

反応手順

2,3-dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo[1,2-a]pyridine-6-carboxylic acid (0.3 g, 0.88 mmol) and o-Benzotriazol-1-yl-N,N,N′,N′-Tetramethyluronium tetrafluoroborate (TBTU)(0.29 g, 0.90 mmol) were added to methylene chloride (15 ml) and the mixture was stirred for 5 min. Ethanolamin (0.11 g, 1.8 mmol) was added and the reaction mixture was stirred at ambient temperature for 2 h. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography on silica gel using methylene chloride:methanol (9:1) as eluent. Crystallization from diethyl ether gave 0.2 (59%) 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-42b48ea3bdba48d2a2a91ebd18ff3312
出典メモuspto-grants-2001_11