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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893663Generated: October 30, 2026

Potassium Iodide → HCID 13587988, compound

https://huagongshe.com/reaction/893663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantPicolyl chloride hydrochlorideHCID 23392—
Reactant1-Piperidinecarboxylic acid, 4-(1H-benzimidazol-2-ylamino)-, ethyl esterHCID 3018455—
SolventDimethylformamideHCID 6228—
ProductHCID 13587988HCID 1358798840%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 57.5 parts of ethyl 4-(1H-benzimidazol-2-ylamino)-1-piperidinecarboxylate, 33 parts of 2-(chloromethyl)pyridine hydrochloride, 43 parts of sodium carbonate, 0.1 parts of potassium iodide and 630 parts of N,N-dimethylformamide was stirred and heated overnight at 70° C. The reaction mixture was cooled and poured onto water. The product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (96:4 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized form 4-methyl-2-pentanone, yielding 30 parts (40%) of ethyl 4-[[1-[(2-pyridinyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinecarboxylate; mp. 161.5° C. (intermediate 60).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05126339
Source datasetuspto-grants-1992_06
ORD IDord-377bfd9d83124b6284e7d5d2ee39ec2d
Source noteuspto-grants-1992_06