Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252341Generated: October 31, 2026

3-Methoxypropyne → HCID 23156218, compound

https://huagongshe.com/reaction/252341

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxypropyneHCID 69393—
Reactant5-bromo-3-iodo-1-methyl-1H-indazoleHCID 23156226—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 23156218HCID 23156218—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 81.67 g of 5-bromo-3-iodo-1-methyl-1H-indazole in 750 ml of N,N-dimethylformamide and 335 ml of triethylamine is admixed at room temperature under argon with 25 ml of 3-methoxypropyne, 5.5 g of copper(I) iodide and 10 g of bis(triphenylphosphine)palladium(II) chloride, and subsequently heated to 60° C. After 1 hour, the reaction mixture is cooled to room temperature, diluted with water and extracted with ethyl acetate (4×). The combined organic phases are dried over sodium sulphate and concentrated by evaporation. The title compound is obtained as a yellow solid from the residue by means of flash chromatography (SiO2 60F). Rf=0.67 (2:1 EtOAc-heptane). Rt=4.42 (gradient I).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868036B2
Source datasetuspto-grants-2011_01
ORD IDord-a8f90e61a1e54e63b8cd5e5ce3954a41
Source noteuspto-grants-2011_01