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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1029563Erstellt: 25. Oktober 2026

Butyric Acid → 5-Butyramido-2-propylimidazo[4,5-b]pyridine

https://huagongshe.com/reaction/1029563

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButyric AcidHCID 264—
EduktDichloromethaneHCID 6344—
Edukt2,6-Diamino-3-nitropyridineHCID 319998—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelAmmonium HydroxideHCID 14923—
Produkt5-Butyramido-2-propylimidazo[4,5-b]pyridineHCID 2240738149,1%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 2,6-diamino-3-nitropyridine (878 mg, 5.7 mmol) and Pd-C (10%, 100 mg) in MeOH (100 mL) was stirred under 1 atm. H2 for 16 hours. The mixture (containing the air sensitive triamine) was filtered, evaporated, and to this flask was added polyphosphoric acid (15 mL) and butyric acid (1.05 mL, 11.5 mmol). This mixture was heated to 80° C. for 5 hours, cooled to room temperature, diluted with water and neutralized with concentrated NH4OH. Extractive workup (CH2Cl2) gave 345 mg of 5-(butyramido)-2-propylimidazo[4,5-b]pyridine: 1H NMR (300 MHz, CDCl3) δ7.94 (d, 1H, J=8.5 Hz), 7.65 (d, 1H, J=8.5 Hz), 2.96 (t, 2H J=7.5 Hz), 2.30 (t, 2H J=7 Hz), 1.98-1.84 (m, 2H), 1.68-1.55 (m, 2H), 0.99 (t, 3H, J=7.5 Hz), 0.80 (t, 3H, J=7.0 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05102880
Quelldatensatzuspto-grants-1992_04
ORD IDord-4ed784dc78a24cd2938997a23c8937e8
Quellennotizuspto-grants-1992_04