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HRID 1655865Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1655865

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPhosphorus oxychlorideHCID 24813—
EduktChloro-N,N-dimethylformiminium chlorideHCID 77311—
EduktDimethyl [(1-methylpyrazol-4-yl)amino]butenedicarboxylateHCID 19417344—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt1h-Pyrazolo[4,3-b]pyridine-5,6-dicarboxylic acid,1-methyl-,5,6-dimethyl esterHCID 1995821671,4%

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05252538
Quelldatensatzuspto-grants-1993_10
ORD IDord-a40124204ac942658184d44ca2fb6d51
Quellennotizuspto-grants-1993_10