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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354150Generated: October 29, 2026

Sodium Carbonate → 2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-(1-(3-(1,3-dihydro-2H-benzimidazol-2-one-1-yl)propyl)piperidine-4yl)acetamide

https://huagongshe.com/reaction/354150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 1810419—
Reactant2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-(piperidin-4-yl)acetamideHCID 9946526—
SolventAcetonitrileHCID 6342—
Product2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-(1-(3-(1,3-dihydro-2H-benzimidazol-2-one-1-yl)propyl)piperidine-4yl)acetamideHCID 10119088—

Reaction Conditions

Temperature82 °C

Reaction Steps

50ELH87 (0.05 g, 0.14 mmol, 1 eq.) was transferred to a 4 ml vial and dissolved in 1 ml of acetonitrile. Then, 1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one (0.032 g, 1.1 eq.), sodium carbonate (0.022 g, 1.1 eq.) and KI (one crystal) were added and the vial was sealed and shaken for 20 h at 82° C. The mixture was extracted with distilled water (pH 10, sodium carbonate) and dichloromethane (3 times) the organic layers were dried with sodium sulfate and concentrated. The title compound was purified by HPLC and evaporated to dryness, forming a trifluoroacetic acid salt. Yield 8.8 mg (12%). UV/MS 100/100 (M+ 527), rt (A, MS) 2.851.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756393B2
Source datasetuspto-grants-2004_06
ORD IDord-bea640ab1acd47c7a4c56e9259385eb8
Source noteuspto-grants-2004_06