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HRID 427490作成日:2026年10月25日

Potassium Iodide → 2,3-Dimethyl-8-(2,6-dimethyl-4-fluoro-benzylamino)-imidazo[1,2-a]pyridine-6-carboxamide mesylate

https://huagongshe.com/reaction/427490

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物DiisopropylethylamineHCID 81531—
反応物8-Amino-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxamide mesylateHCID 18357435—
反応物2-(Bromomethyl)-5-fluoro-1,3-dimethylbenzeneHCID 22672641—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物2,3-Dimethyl-8-(2,6-dimethyl-4-fluoro-benzylamino)-imidazo[1,2-a]pyridine-6-carboxamide mesylateHCID 1835742824%

反応手順

8-Amino-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxamide mesylate (5.0 g, 13.4 mmol), 2,6-dimethyl-4-fluorobenzylbromide (2.91 g, 13.4 mmol), diisopropylethylamin (3.8 g, 29.5 mmol) and a cat. amount of potassium iodide were stirred in dimethylformamide (20 ml) at room temperature overnight. Water (70 ml) and methylene chloride (2×50 ml) were added to the reaction mixture and the organic layer was separated, dried and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using methylene chloride:methanol (9:1) as eluent. The product was solved in isopropanol and methansulfonic acid (0.3 g) was added. The salt that formed was isolated by filtration and washed with isopropanol and diethyl ether to give 1.4 g (24%) of the title compound.

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-a4b2a0765c7648a995700ffb6597e00f
出典メモuspto-grants-2001_11