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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255884Generated: October 26, 2026

Triethylamine → [1-(4-Methoxyphenyl)ethyl]-2-methylpteridin-4-yl-amine

https://huagongshe.com/reaction/1255884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,4-Dioxane-2,3-diolHCID 96170—
Reactant1-(4-Methoxyphenyl)ethanamineHCID 238181—
Reactant6-Chloro-2-methylpyrimidine-4,5-diamineHCID 594145—
SolventEthanolHCID 702—
SolventEthyl acetate hexaneHCID 21226206—
Product[1-(4-Methoxyphenyl)ethyl]-2-methylpteridin-4-yl-amineHCID 5817422821.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 6-chloro-4,5-diamino-2-methylpyrimidine (317 mg, 2.0 mmol) and 1,4-dioxane-2,3-diol (240 mg, 2.0 mmol) in EtOH (15 mL) was stirred at 25° C. for 1 h. TLC analysis (1:1 hexane/EtOAc on SiO2) indicated complete consumption of starting material. 1-(4-Methoxyphenyl)-ethylamine (332 mg, 2.2 mmol) and triethylamine (Et3N, 0.3 mL, 2.2 mmol) were added, and the reaction was stirred overnight. The majority of solvent was removed in vacuo and the residue was partitioned between EtOAc and H2O. The organic layer was concentrated in vacuo to leave a brown residue that was purified by column chromatography over SiO2, eluting with 2:1 EtOAc/hexane, then 100% EtOAc to afford [1-(4-methoxyphenyl)ethyl]-2-methylpteridin-4-yl-amine (126 mg) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461164B2
Source datasetuspto-grants-2013_06
ORD IDord-2d652c990f454b36b30dbadce40fb6c8
Source noteuspto-grants-2013_06