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HRID 1092008作成日:2026年10月26日

4-Fluorobenzoic Acid → HCID 178489757、化合物

https://huagongshe.com/reaction/1092008

反応式

関与物質

役割名称HCID仕込み量
反応物4-Fluorobenzoic AcidHCID 9973—
反応物Oxalyl chlorideHCID 65578—
反応物DiisopropylethylamineHCID 81531—
反応物HCID 178489815HCID 178489815—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物HCID 178489757HCID 1784897573%

反応条件

温度0 °C

反応手順

Oxalyl chloride (2M in DCM, 1.40 ml, 2.75 mmol, 1.1 eq) was added dropwise to a mixture of 4-fluorobenzoic acid (350 mg, 2.50 mmol, 1 eq) in dichloromethane (15 ml) at 0° C. containing a few drops of DMF (10 ul, 0.12 mmol, 0.05 eq) and DIPEA (937 μl, 5.25 mmol, 2.1 eq). After stirring for 60 mins at 0° C. a solution of 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (742 mg, 3 mmol, 1.2 eq) in DCM (10 ml) was added dropwise over 15 mins. The mixture was maintained at 0° C. for a further 2 h, then gradually allowed to warm to room temperature overnight. The mixture was diluted with DCM (50 ml) and washed with aqueous NaHCO3 solution (50 ml). The aqueous layer was extracted with DCM (50 ml). The combined organic layers were collected and concentrated. The crude product was purified by reverse-phase prep HPLC using a 30-50% gradient of acetonitrile in water containing 1% ammonium hydroxide solution. The desired fractions were evaporated to afford the title compound as a beige solid. (31.5 mg, 3% yield)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08129391B2
出典データセットuspto-grants-2012_03
ORD IDord-256d18a37524478297e73a184d4cd89b
出典メモuspto-grants-2012_03