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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446348Generated: October 30, 2026

N,N-Dimethylpropargylamine → HCID 58588457, compound

https://huagongshe.com/reaction/446348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylpropargylamineHCID 81643—
ReactantHCID 66970357HCID 66970357—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178419050HCID 178419050—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 58588457HCID 58588457—

Reaction Steps

A mixture of 3-iodo-N-(3-methyl-4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)benzamide (0.20 g, 0.37 mmol), N,N-dimethylprop-2-yn-1-amine (0.080 mL, 0.74 mmol), bis(triphenylphosphine)palladium (II) dichloride (0.013 g, 0.020 mmol), copper (I) iodide (0.0035 g, 0.020 mmol) in triethylamine (1.5 mL) and acetonitrile (5 mL) was heated in a sealed tube to 100 deg. C. for 3.5 h. The reaction was diluted in dichloromethane and filtered. The filtrate was concentrated in vacuo and the resulting material was purified by silica gel chromatography using MeOH/dichloromethane as eluent to give 3-(3-(dimethylamino)prop-1-ynyl)-N-(3-methyl-4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)benzamide as a brown solid. MS m/z=493 [M+1]+. Calc'd for C29H28N6O2: 492.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476434B2
Source datasetuspto-grants-2013_07
ORD IDord-b2ae6dd547f940a38b43a195f2c8a06f
Source noteuspto-grants-2013_07