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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437633Generated: October 30, 2026

5-Chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one → HCID 21428799, compound

https://huagongshe.com/reaction/437633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-oneHCID 104607—
ReactantN-(2-Bromoethyl)-2-nitrobenzene-1-carboximidic acidHCID 3017373—
SolventDimethylformamideHCID 6228—
ProductHCID 21428799HCID 2142879967%

Reaction Steps

A mixture of 1.5 parts of N-(2-bromoethyl)-2-nitrobenzamide, 1.55 parts of 5-chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one and 27 parts of N,N-dimethylformamide is stirred and refluxed for 5 hours. The reaction mixture is evaporated and the oily residue is crystallized from ethanol. The product is filtered off and dried, yielding 2.2 parts (67%) of N-{2-[4-(5-chloro-2,3-dihydro-2-oxo- 1H-benzimidazol-1-yl)-1-piperidinyl] ethyl}-2-nitrobenzamide hydrobromide. hemihydrate; mp. 273.2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031226
Source datasetuspto-grants-1977_06
ORD IDord-c3f6cfc090ed4d929007242e546b3cfe
Source noteuspto-grants-1977_06