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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071994Generated: October 25, 2026

Cuminaldehyde → 4-(4-isopropylphenyl)-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine

https://huagongshe.com/reaction/1071994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCuminaldehydeHCID 326—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178478691HCID 178478691—
SolventEthanolHCID 702—
Product4-(4-isopropylphenyl)-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridineHCID 311674194.9%

Reaction Steps

A mixture of histamine dihydrochloride (1.85 g, 10.0 mmol), water (10 mL), potassium hydroxide (1.72 g, 30.0 mmol), ethanol (25 mL) and 4-isopropylbenzaldehyde (1.62 g, 10.91 mmol) was heated to reflux for 1.5 h. Ethanol was evaporated and the residue was diluted with water (40 mL). Extraction (5×25 mL DCM), washing of the combined extracts (2×50 mL brine) and drying (MgSO4) yielded 2.29 g (87%) of crude 4-(4-isopropylphenyl)-4,5,6,7-tetrahydro-imidazo[4,5-c]pyridine, which was used for the next synthetic step without further purification. This amine (0.48 g, 1.99 mmol) was dissolved in DCM (5 mL) and added to a 30 min old mixture of 3-(4-fluorophenyl)propionic acid (0.31 g, 1.84 mmol), HOBt (0.27 g, 1.20 mmol) and EDC (0.42 g, 12.19 mmol) in DCM (10 mL). After 18 h the mixture was washed with water (50 mL), dried (MgSO4) and concentrated. The crude product was purified by column chromatography (silica gel, gradient elution with DCM/methanol). 0.24 g (33%) of the title amide was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908926B1
Source datasetuspto-grants-2005_06
ORD IDord-41a7616a709e43fe9607f9524313d021
Source noteuspto-grants-2005_06