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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958315Generated: October 26, 2026

Toluene → 3,6-dimethyl-N-(2-phenylimidazo[1,2-a]pyrimidin-7-yl)picolinamide

https://huagongshe.com/reaction/1958315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantMethyl 3,6-dimethylpicolinateHCID 10511234—
ReactantTrimethylaluminumHCID 16682925—
Reactant2-Phenylimidazo[1,2-A]pyrimidin-7-amineHCID 50878390—
Solvent1,4-DioxaneHCID 31275—
Product3,6-dimethyl-N-(2-phenylimidazo[1,2-a]pyrimidin-7-yl)picolinamideHCID 5346671143.7%

Reaction Steps

To a white suspension of 2-phenyl-imidazo[1,2-a]pyrimidin-7-ylamine (example 1, step 1, 80 mg, 0.38 mmole) in dioxane (3 ml) is added at RT trimethyl aluminium sol. 2M in toluene (0.8 ml, 1.52 mmole, 4 eq.). The mixture is stirred for 45 min at RT. A solution of 3,6-dimethyl-pyridine-2-carboxylic acid methyl ester (63 mg, 0.38 mmole, 1 eq.) in dioxane (0.4 ml) is then added and the light brown solution is refluxed overnight. The brown solution is loaded on 2 g silica and purified by chromatography on a 12 g RediSep silica cartridge (eluent heptane/ethyl acetate 30-70% 15 min) affording 3,6-dimethyl-N-(2-phenylimidazo[1,2-a]pyrimidin-7-yl)picolinamide (57 mg, 43.6%) as a white solid. MS (m/e)=344.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410117B2
Source datasetuspto-grants-2013_04
ORD IDord-d232d4280e7c42dd80fa86105863e6c7
Source noteuspto-grants-2013_04