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HRID 559684作成日:2026年10月26日

Water → {[1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carbonyl]amino}-acetic acid methyl ester

https://huagongshe.com/reaction/559684

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物Glycine methyl ester hydrochlorideHCID 122755—
反応物1-(4-Fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acidHCID 59278137—
溶媒DimethylformamideHCID 6228—
溶媒Ammonium BicarbonateHCID 14013—
生成物{[1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carbonyl]amino}-acetic acid methyl esterHCID 66727434—

反応手順

A suspension of 1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid (2.95 g, 11.5 mmol) in DMF (25 mL) was treated with CDI (1.51 g, 12.0 mmol). The mixture turned to a dark brown clear solution in 5 minutes, and then a solid precipitate formed. Additional DMF (10 mL) was added to assist stirring. The mixture was stirred for 1 hour. A solution of glycine methyl ester hydrochloride (2.42 g, 14.9 mmol) in DMF (5 mL) was added. After 18 hours, the mixture was poured into water (200 mL) and diluted with saturated aqueous ammonium bicarbonate (50 mL). The solid was collected by filtration to afford {[1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carbonyl]-amino}-acetic acid methyl ester as a light brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063065B2
出典データセットuspto-grants-2011_11
ORD IDord-6f78f9f354144ae98f9765fed484a4e6
出典メモuspto-grants-2011_11