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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668465Generated: October 30, 2026

Indole → HCID 18005067, compound

https://huagongshe.com/reaction/1668465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantWaterHCID 962—
ReactantN,N'-DimethylethylenediamineHCID 8070—
Reactant3-BromopyridineHCID 12286—
ReactantPotassium Phosphate, TribasicHCID 62657—
CatalystCopper iodideHCID 83717—
SolventTolueneHCID 1140—
ProductHCID 18005067HCID 1800506767.9%

Reaction Conditions

Temperature110 °C

Reaction Steps

A suspension of compound 1 (195 mg, 1.20 mmol), 3-Bromopyridine (98 μL, 1.00 mmol), copper iodide (9.5 mg, 0.05 mmol) and K3PO4 (400 mg, 2.10 mmol) in toluene (6 mL) was treated with N,N′-dimethylethylenediamine (21.5 μL, 0.20 mmol) then heated at 110° C. overnight. A TLC analysis indicated mostly starting indole and 3-bromopyridine and a new more polar spot. The reaction mixture was treated with additional copper iodide ((9.5 mg, 0.05 mmol) and N,N′-dimethylethylenediamine (21.5 μL, 0.20 mmol). The mixture was heated at 110° C. for 7 hours. After cooling, the mixture was poured into H2O (20 mL) then extracted with CH2Cl2 (100 mL). The organic layer was separated, washed with brine and concentrated to give a yellow solid which was subjected to flash chromatography on silica gel (CH2Cl2 to MeOH:CH2Cl2, 5:95) to give compound 72 (195 mg, 67.9%) as a yellow solid. 1H NMR (DMSO-d6) δ 8.90 (d, J=2.4 Hz, 1H), 8.70-8.69 (m, 2H), 8.16-8.07 (m, 2H), 7.99 (d, J=3.2 Hz, 1H), 7.71-7.65 (m, 2H), 7.05 (d, J=3.3 Hz); ESI-MS (m/z, %): 240 (M+1, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989447B2
Source datasetuspto-grants-2011_08
ORD IDord-4f849f1d3387499faecd3dfcc313eb75
Source noteuspto-grants-2011_08