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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198755Generated: October 31, 2026

Ammonia → HCID 13056042, compound

https://huagongshe.com/reaction/2198755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(4-Piperidinyl)-1H-indoleHCID 702235—
Reactant1-(4-chlorobutyl)-1,3-dihydro-3-(1-methylethenyl)-2H-benzimidazol-2-oneHCID 13016879—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13056042HCID 13056042—

Reaction Steps

A mixture consisting of 3.0 gm of 4-(3-indolyl)-piperidine, 4.0 gm of 1-(4-chloro-butyl)-3-isopropenylbenzimidazolone, 1.3 gm of sodium bicarbonate, 30 ml of dimethyl-formamide and 30 ml of tetrahydrofuran was refluxed for 16 hours. Thereafter, the reaction mixture was poured into a mixture of ice and ammonia, the aqueous mixture was extracted with ethyl acetate, and the extract solution was washed with water, dried and evaporated to dryness in vacuo. The residue was dissolved in ether, etheric hydrogen chloride was added to the solution, and the precipitate formed thereby was collected by filtration, dried and dissolved in 100 ml of ethanol. The resulting solution was cooled, 16 ml of concentrated sulfuric acid were carefully added while stirring, and the mixture was allowed to stand at 20° C. for two hours, whereupon it was poured into a mixture of ice and ammonia. The precipitate formed thereby was collected by filtration and recrystallized from ethanol, yielding 3.2 gm (55% of theory) of the compound of the formula ##STR13## having a melting point of 196° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04359468
Source datasetuspto-grants-1982_11
ORD IDord-3cd6460e83eb40b191b9c1cbccb2648e
Source noteuspto-grants-1982_11