Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271040Generated: October 26, 2026

Triethylamine → 5-(4-Bromophenylethynyl)-4-chloro-2-diisopropylaminomethyleneaminopyrimidine

https://huagongshe.com/reaction/1271040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzene, 1-bromo-4-ethynyl-HCID 136603—
Reactant4-Chloro-2-diisopropylaminomethyleneamino-5-iodopyrimidineHCID 73446451—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product5-(4-Bromophenylethynyl)-4-chloro-2-diisopropylaminomethyleneaminopyrimidineHCID 7344645678.1%

Reaction Steps

A mixture of 0.5 g of 1-bromo-4-ethynylbenzene, 5.0 mL of triethylamine, 0.031 mg of copper iodide, 0.94 g of 4-chloro-2-diisopropylaminomethyleneamino-5-iodopyrimidine and 0.046 g of dichlorobis(triphenyl)phosphine palladium II was magnetically stirred at room temperature for 18 hrs. The mixture was diluted with acetonitrile, filtered and the filtrate evaporated in vacuo. The evaporated filtrate was dissolved in dichloromethane and loaded on a column of silica gel equilibrated in the same solvent. Cuts were monitored by thin layer chromatography. After initial cuts of brown colored eluates, the product subsequently eluted as yellow fractions. Like cuts were pooled and evaporated to give 0.84 g of 5-(4-bromophenylethynyl)-4-chloro-2-diisopropylaminomethyleneaminopyrimidine as a thick amber syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205297B2
Source datasetuspto-grants-2007_04
ORD IDord-6ec0d97fa2584cd3b1674bb15858e107
Source noteuspto-grants-2007_04