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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396051Generated: October 25, 2026

4-[(2S)Oxiranylmethoxy]-1,3-dihydro-2H-benzimidazol-2-one → 4-(4-(2-[(2S)-2-Hydroxy-3-(2-oxo-2,3-dihydro-1H-benzoimidazol-4-yloxy)-propylamino]-ethoxy}-phenylamino)-piperidine-1-carboxylic acidoctylamide

https://huagongshe.com/reaction/396051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(2S)Oxiranylmethoxy]-1,3-dihydro-2H-benzimidazol-2-oneHCID 10512450—
Reactant4-[4-(2-Aminoethoxy)anilino]-N-octyl-1-piperidinecarboxamide formateHCID 69987684—
SolventChloroform methanolHCID 21584188—
Product4-(4-(2-[(2S)-2-Hydroxy-3-(2-oxo-2,3-dihydro-1H-benzoimidazol-4-yloxy)-propylamino]-ethoxy}-phenylamino)-piperidine-1-carboxylic acidoctylamideHCID 1014530219.4%

Reaction Steps

4-[4-(2-Aminoethoxy)anilino]-N-octyl-1-piperidinecarboxamide formate (0.32 g, 0.733 mmol) was reacted with 4-[(2S)oxiranylmethoxy]-1,3-dihydro-2H-benzimidazol-2-one (0.151 g, 0.732 mmol) according to Procedure G (eluant: 20:1 chloroform-methanol) to give the title compound (0.085 g, 0.142 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605618B2
Source datasetuspto-grants-2003_08
ORD IDord-a9379cfb1a1749dea611d3ca35215633
Source noteuspto-grants-2003_08