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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524657Generated: October 25, 2026

4-Chloro-1H-pyrrolo[2,3-b]pyridine → 4-(4-Phenyl-1H-imidazol-1-yl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1524657

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 11389493—
ReactantHCID 178418822HCID 178418822—
Product4-(4-Phenyl-1H-imidazol-1-yl)-1H-pyrrolo[2,3-b]pyridineHCID 17754409291%

Reaction Steps

A melt of 4-chloro-1H-pyrrolo[2,3-b]pyridine (0.050 g, 0.00033 mol) in 4-phenyl-1H-imidazole (0.24 g, 0.0016 mol) was heated at 200° C. overnight. The reaction was partitioned between ethyl acetate and saturated NaHCO3, separated and the organic phase was washed with brine. The organic layer was then dried and evaporated to give 250 mg of an orange oil. The oil was chromatographed with 7% MeOH/DCM, 0.7% NH4OH, sample in solvent system. Collected 74 mg of the product as an orange glass. The glass was triturated with hot DCE (1.5 mL) to give 51 mg of a brown solid which was dried at 60° C. for 4 h to afford the desired product (50 mg, 59 yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079912B2
Source datasetuspto-grants-2015_07
ORD IDord-183d4c9afafb44dda547e475e9f50ff1
Source noteuspto-grants-2015_07