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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347905Generated: October 25, 2026

Pyridine → 1-Phenyl-1H-pyrrolo[3,2-b]pyridine

https://huagongshe.com/reaction/347905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
Reactant4-AzaindoleHCID 9226—
ReactantPhenylboronic AcidHCID 66827—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Product1-Phenyl-1H-pyrrolo[3,2-b]pyridineHCID 2108396339.5%

Reaction Steps

1H-Pyrrolo[3,2-b]pyridine (0.5 g, 4.24 mmol), phenylboronic acid (1.03 g, 8.44 mmol), copper(II) acetate (1.54 g, 8.48 mmol), and 4A molecular sieves (2 g), were suspended in DCM (10 mL). Triethylamine (1.19 mL, 8.5 mmol) and pyridine (0.7 mL, 8.65 mmol) were added and the reaction stirred at r.t. for three days. The reaction mixture was diluted with further DCM, filtered and concentrated in vacuo. Chromatography (silica, EtOAc) gave the title compound (325 mg). δH (CDCl3) 7.80 (1H, d, J 8.2 Hz), 7.54–7.30 (7H, m), 7.15 (1H, brs), 6.88 (1H, brs). LCMS (ES+) RT 1.20 minutes, 195 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176215B2
Source datasetuspto-grants-2007_02
ORD IDord-2f4441f43afe4a7a8bcb4cfbf57ac8f6
Source noteuspto-grants-2007_02