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HRID 23623作成日:2026年10月25日

Water → 4-(2-amino-2-oxoethyl)-N-(4-chlorobenzyl)-2-(hydroxymethyl)-3-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide

https://huagongshe.com/reaction/23623

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物IodoacetamideHCID 3727—
反応物Potassium CarbonateHCID 11430—
反応物HCID 178429625HCID 178429625—
溶媒DimethylformamideHCID 6228—
生成物4-(2-amino-2-oxoethyl)-N-(4-chlorobenzyl)-2-(hydroxymethyl)-3-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 2257436856.1%

反応条件

温度50 °C

反応手順

A mixture of N-(4-chlorobenzyl)-7-hydroxy-2-(hydroxymethyl)-3-methylthieno[3,2-b]pyridine-6-carboxamide (100 mg, 0.276 mmol), potassium carbonate (57 mg, 0.41 mmol) and iodoacetamide (255 mg, 1.38 mmol) in DMF (1.5 mL) was stirred at 50° C. for 18 hrs. Additional iodoacetamide (255 mg) and potassium carbonate (57 mg) were added, and the reaction was stirred at the same temperature for another 12 hrs. After cooling, cold water was added, and the resulting ppt was collected by filtration after chilling in an ice bath. The collected crude solid was recrystallized from aq. ethanol to give the title compound (65 mg) as a lt. brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852731B2
出典データセットuspto-grants-2005_02
ORD IDord-a2a3ee5c1f5d4061bd2b4e9afb037b1c
出典メモuspto-grants-2005_02