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HRID 5441作成日:2026年10月23日

Formaldehyde → 5-[2-(Methylsulfonylamino)ethylthio]3-morpholinomethylimidazo[1,2-a]pyridine

https://huagongshe.com/ja/reaction/5441

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物MorpholineHCID 8083—
反応物5-[2-(Methylsulfonylamino)ethylthio]imidazo[1,2-a]pyridineHCID 15229363—
溶媒Acetic AcidHCID 176—
生成物5-[2-(Methylsulfonylamino)ethylthio]3-morpholinomethylimidazo[1,2-a]pyridineHCID 2336285171.5%

反応手順

To a solution of 37% formalin (178 mg, 2.2 mmoles) in acetic acid (2 ml) was added morpholin (192 μl, 2.2 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. 5-[2-(methylsulfonylamino)ethylthio] imidazo[1,2-a]pyridine (543 mg, 2 mmoles) was added to the reaction mixture, followed by stirring at 60° C. for 2 hours. After the solvent was distilled off, the residue was dissolved in chloroform (50 ml) and washed with 1N NaOH (10 ml). Then, the aqueous layer was extracted with chloroform (30 ml×3) and the combined chloroform layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:10→1:5) to obtain 530 mg of the desired product (71.5%, colorless solid).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244908
出典データセットuspto-grants-1993_09
ORD IDord-1c9d4fa8cda74077a9d8cdb9265be8ed
出典メモuspto-grants-1993_09