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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203113Generated: October 29, 2026

1,2-Dimethoxyethane → 1-(2-Cyclopropyl-1-methyl-1h-benzimidazol-6-yl)-4-[(2-cyclopropyl-4-thiazolyl)methoxy]-2(1h)-pyridinone

https://huagongshe.com/reaction/2203113

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant4-[(2-Bromo-4-thiazolyl)methoxy]-1-(2-cyclopropyl-1-methyl-1h-benzimidazol-6-yl)-2(1h)-pyridinoneHCID 121386271—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product1-(2-Cyclopropyl-1-methyl-1h-benzimidazol-6-yl)-4-[(2-cyclopropyl-4-thiazolyl)methoxy]-2(1h)-pyridinoneHCID 8970267124.7%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 4-((2-bromo-1,3-thiazol-4-yl)methoxy)-1-(2-cyclopropyl-1-methyl-1H-benzimidazol-6-yl)pyridin-2(1H)-one (54 mg), cyclopropylboronic acid (30.4 mg), tetrakis(triphenylphosphine)palladium (6.8 mg), potassium carbonate (65.3 mg), DME (1.5 ml) and water (0.5 ml) was heated at 150° C. for 20 min under microwave irradiation. The reaction mixture was then cooled to room temperature, poured into water and extracted with EtOAc. The extract was washed with brine, dried over MgSO4, concentrated and purified by silica gel column chromatography (hexane/EtOAc then EtOAc/MeOH). The resulting solid was recrystallized from EtOH-water to give the title compound (12.2 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365540B2
Source datasetuspto-grants-2016_06
ORD IDord-5f03c5b2eb8f4846b2337238d99457e3
Source noteuspto-grants-2016_06