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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678141Generated: November 1, 2026

Pyridine → HCID 46912083, compound

https://huagongshe.com/reaction/1678141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-Chloro-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehydeHCID 46941713—
SolventDichloromethaneHCID 6344—
ProductHCID 46912083HCID 4691208325%

Reaction Steps

A mixture of 2-chloro-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehyde (70 mg, 0.39 mmol) cupric acetate (140 mg, 0.77 mmol), phenylboronic acid (93 mg, 0.76 mmol), 4A molecular sieve (200 mg), triethylamine (106 μl), pyridine (61 μL) and dichloromethane (5.5 mL) is vigorously stirred at room temperature for 48 hr. The solids are removed by filtration through a pad of Hi-Flo and the filtrate is concentrated. The residue is purified by chromatography eluting with dichloromethane-2% methanol. Product containing fractions are combined and concentrated to give 2-chloro-1-phenyl-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehyde (25 mg, 25% yield) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008491B2
Source datasetuspto-grants-2011_08
ORD IDord-e237e1a52e334dfebd799ae6ccdfb027
Source noteuspto-grants-2011_08