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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029563Generated: October 25, 2026

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

https://huagongshe.com/reaction/1029563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyric AcidHCID 264—
ReactantDichloromethaneHCID 6344—
Reactant2,6-Diamino-3-nitropyridineHCID 319998—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventAmmonium HydroxideHCID 14923—
Product5-Butyramido-2-propylimidazo[4,5-b]pyridineHCID 2240738149.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102880
Source datasetuspto-grants-1992_04
ORD IDord-4ed784dc78a24cd2938997a23c8937e8
Source noteuspto-grants-1992_04