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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437632Generated: October 30, 2026

Methanol → HCID 86734881, compound

https://huagongshe.com/reaction/437632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantOxalic AcidHCID 971—
Reactant1,3-Dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-oneHCID 88638—
ReactantHCID 21428987HCID 21428987—
SolventAcetoneHCID 180—
SolventBenzeneHCID 241—
ProductHCID 86734881HCID 86734881—

Reaction Steps

A mixture of 1.75 parts of 1-(2-methoxy-benzoyl)aziridine, 2.18 parts of 1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one, 1.6 parts of methanol and 10.8 parts of benzene is stirred and refluxed for 1.50 hours. The reaction mixture is cooled. After the addition of 2-propanone, the whole is acidified with ethanedioic acid. The formed ethanedioate salt is filtered off and crystallized from ethanol 70%, yielding 2.9 parts of N-{2-[4-(2,3-dihydro-2-oxo-1 H-benzimidazol-1-yl)-1-piperidinyl] ethyl}-2-methoxybenzamide ethanedioate; mp. 217.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031226
Source datasetuspto-grants-1977_06
ORD IDord-18bb0b82316341e0838e7b33f1c98bfa
Source noteuspto-grants-1977_06