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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856574Generated: October 25, 2026

Potassium Iodide → 1-(4-fluorophenylmethyl)-N-{1-[2-(4-morpholinyl)ethyl]-4-piperidinyl}-1H-benzimidazol-2-amine trihydrochloride

https://huagongshe.com/reaction/1856574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMorpholineHCID 8083—
ReactantN-[1-(2-chloroethyl)-4-piperidinyl]-1-(4-fluorophenylmethyl)-1H-benzimidazol-2-amine dihydrochlorideHCID 12891728—
SolventDimethylformamideHCID 6228—
Product1-(4-fluorophenylmethyl)-N-{1-[2-(4-morpholinyl)ethyl]-4-piperidinyl}-1H-benzimidazol-2-amine trihydrochlorideHCID 2334515318.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 3.6 parts of morpholine, 4.8 parts of N-[1-(2-chloroethyl)-4-piperidinyl]-1-(4-fluorophenylmethyl)-1H-benzimidazol-2-amine dihydrochloride, 0.1 parts of potassium iodide and 135 parts of N,N-dimethylformamide is stirred and heated overnight at 70° C. The reaction mixture is poured onto water and the product is extracted with methylbenzene. The extract is dried, filtered and evaporated. The residue is converted into the hydrochloride salt in methanol. The salt is filtered off and dried, yielding 1 part (18.3%) of 1-(4-fluorophenylmethyl)-N-{1-[2-(4-morpholinyl)ethyl]-4-piperidinyl}-1H-benzimidazol-2-amine trihydrochloride; mp.+300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04219559
Source datasetuspto-grants-1980_08
ORD IDord-eb56b0dfcc404ad98adaa01d9e22b8f9
Source noteuspto-grants-1980_08