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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486822Generated: October 26, 2026

N,N'-Dimethylethylenediamine → 1-(4-Chlorophenyl)-1H-pyrrolo[2,3-c]pyridine

https://huagongshe.com/reaction/1486822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
Reactant6-AzaindoleHCID 9219—
Reactant1-Chloro-4-iodobenzeneHCID 12510—
ReactantPotassium Phosphate, TribasicHCID 62657—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
Product1-(4-Chlorophenyl)-1H-pyrrolo[2,3-c]pyridineHCID 5740265688.7%

Reaction Conditions

Temperature150 °C

Reaction Steps

6-Azaindole (5.00 g, 42.3 mmol) was dissolved in DMF (150 mL) under nitrogen and 1-chloro-4-iodo-benzene (12.2 g, 50.8 mmol), N,N′-dimethylethylenediamine (911 uL, 8.46 mmol), K3PO4 (18.9 g, 88.9 mmol) and CuI (806 mg, 4.23 mmol) were added. The reaction mixture was heated at 150° C. for 18 h. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was suspended in 1M aq Na2CO3 (250 mL) and extracted into DCM (2×250 mL). The combined organic fractions were dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography to give the title compound as a yellow solid (8.58 g, 88.6%). LCMS (ES+): 229.1 [MH]+. HPLC: Rt 4.48 min, 98.6% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428498B2
Source datasetuspto-grants-2016_08
ORD IDord-ae685789ab95441f8748070d52557965
Source noteuspto-grants-2016_08