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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951177Generated: November 4, 2026

Imidazole → [5-(2-Imidazol-1-yl-pyridin-4-yl)-4-methyl-thiazol-2-yl]-pyrazin-2-yl-amine

https://huagongshe.com/reaction/1951177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantCesium carbonateHCID 10796—
Reactant[5-(2-Chloro-pyridin-4-yl)-4-methyl-thiazol-2-yl]-pyrazin-2-yl-amineHCID 11301149—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product[5-(2-Imidazol-1-yl-pyridin-4-yl)-4-methyl-thiazol-2-yl]-pyrazin-2-yl-amineHCID 11232938—

Reaction Conditions

Temperature140 °C

Reaction Steps

A stirred solution of [5-(2-Chloro-pyridin-4-yl)-4-methyl-thiazol-2-yl]-pyrazin-2-yl-amine (Ex. 2b, 0.4 g, 1.32 mmol) in DMSO (10 ml) is treated with imidazole (0.18 g, 2.64 mmol) followed by caesium carbonate (0.86 g, 2.64 mmol). The reaction mixture is heated to 140° C. for 48 hours and then allowed to cool to room temperature. The mixture is diluted with water (100 ml) and extracted with ethyl acetate (4×100 ml). The organics are combined, dried over MgSO4 and the solvent removed in vacuo to yield the crude product as a yellow oil. Purification by chromatography on silica, eluting with ethyl acetate-methanol (9:1) affords the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404684B2
Source datasetuspto-grants-2013_03
ORD IDord-836e663510a7495d90d78c935f503d1f
Source noteuspto-grants-2013_03