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HRID 1655865作成日:2026年10月25日

Dimethylformamide → 1h-Pyrazolo[4,3-b]pyridine-5,6-dicarboxylic acid,1-methyl-,5,6-dimethyl ester

https://huagongshe.com/reaction/1655865

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Phosphorus oxychlorideHCID 24813—
反応物Chloro-N,N-dimethylformiminium chlorideHCID 77311—
反応物Dimethyl [(1-methylpyrazol-4-yl)amino]butenedicarboxylateHCID 19417344—
溶媒1,1-DichloroethaneHCID 6365—
生成物1h-Pyrazolo[4,3-b]pyridine-5,6-dicarboxylic acid,1-methyl-,5,6-dimethyl esterHCID 1995821671.4%

反応条件

温度-5 °C

反応手順

Dimethylformamide (7.4 mL, 0.096 mol) is dissolved in 125 mL dichloroethane and the mixture cooled to -5° C. in an acetone/ice bath. Phosphorous oxychloride (8.9 mL, 0.095 mol) is added in one portion and the clear colorless solution is allowed to warm slowly to room temperature, gradually turning yellow. The unpurified dimethyl [(1-methylpyrazol-4-yl)amino]butenedicarboxylate is dissolved in 75 mL of dichloroethane and added to the chilled Vilsmeier reagent dropwise keeping the reaction temperature below 5° C. The mixture is allowed to warm slowly to room temperature over four hours, and then is heated to reflux for one hour. The mixture is concentrated to a solid which is chromatographed using 3:1 hexanes/ethyl acetate. The fractions containing the desired product are combined and concentrated to give the product as a white solid (16.93 g, 71.4%), melting point 148°-149° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05252538
出典データセットuspto-grants-1993_10
ORD IDord-a40124204ac942658184d44ca2fb6d51
出典メモuspto-grants-1993_10