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HRID 531674作成日:2026年10月26日

Chloroacetamide → 2-(4-(4-(3-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)phenyl)piperazin-1-yl) acetamide

https://huagongshe.com/reaction/531674

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroacetamideHCID 6580—
反応物Sodium BicarbonateHCID 516892—
反応物3-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)-5-(4-(piperazin-1-yl)phenyl)-1-tosyl-1H-pyrrolo[2,3-b]pyridinehydrochlorideHCID 90031507—
溶媒Acetone ethanolHCID 21889777—
生成物2-(4-(4-(3-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)phenyl)piperazin-1-yl) acetamideHCID 11852396249.01%

反応手順

Using similar reaction conditions as described in step-i of example-82A, 3-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)-5-(4-(piperazin-1-yl)phenyl)-1-tosyl-1H-pyrrolo[2,3-b]pyridine hydrochloride (50 mg. 0.077 mmol) was alkylated using 2-chloroacetamide (10 mg, 0.116 mmol) and sodium bicarbonate (20 mg, 0.231 mmol) in acetone/ethanol (5/5 mL) to get 25 mg (49.01% yield) of the titled compound. MS: m/z=663.7 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09353107B2
出典データセットuspto-grants-2016_05
ORD IDord-ebfe17bcadb648a2889d21e9d693245b
出典メモuspto-grants-2016_05