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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188811Generated: October 25, 2026

Water → methyl 1-[(3,4-dimethylphenyl)methyl]-2-methyl-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylate

https://huagongshe.com/reaction/1188811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3,4-Dimethylbenzyl chlorideHCID 66018—
ReactantHCID 178498372HCID 178498372—
SolventDimethylformamideHCID 6228—
Productmethyl 1-[(3,4-dimethylphenyl)methyl]-2-methyl-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylateHCID 6710219876%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 2-methyl-5-(4-morpholinyl)-1H-benzimidazole-7-carboxylate prepared as described in Example 26, step d (0.22 g, 0.799 mmol) in N,N-Dimethylformamide (DMF) (10 mL) was added in 4-(chloromethyl)-1,2-dimethylbenzene (0.185 g, 1.199 mmol) and potassium carbonate (0.331 g, 2.397 mmol). The resulting reaction mixture was stirred at 80° C. for 3 h. It was cooled to room temperature and poured into water (30 mL). The mixture was extracted with EtOAc (50 mL×3). The combined organic phases were washed with brine (50 mL) and concentrated. The crude material was subjected to normal phase purification (0˜40% EtOAc/Hexane) then (0˜1% MeOH/DCM) to give the product (0.24 g, 76%). MS (ES+) m/e 394.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674090B2
Source datasetuspto-grants-2014_03
ORD IDord-e112f910363345f6b1a3e4b84fd16e0f
Source noteuspto-grants-2014_03