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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166144Generated: November 2, 2026

Water → HCID 131716479, compound

https://huagongshe.com/reaction/2166144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant3-Furoic acidHCID 10268—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
ReactantHCID 15718930HCID 15718930—
SolventDichloromethaneHCID 6344—
ProductHCID 131716479HCID 13171647936.1%

Reaction Steps

To a stirred mixture of 1.12 parts of 3-furancarboxylic acid, 2.02 parts of N,N-diethylethanamine and 195 parts of dichloromethane were added 2.6 parts of 2-chloro-1-methylpyridinium iodide at room temperature. After stirring for 1 hour, 3.3 parts of N-[1-(2-aminoethyl)-4-piperidinyl]-3-(2-ethoxyethyl)-3H-imidazo[4,5-b]pyridin-2-amine were added and stirred overnight at room temperature. The mixture was poured into water and the layers were separated. The organic layer 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 converted into the ethanedioate salt in ethanol. The salt was filtered off and dried, yielding 2.19 parts (36.1%) of N-[2-[4-[[3-(2-ethoxyethyl)-3H-imidazo[4,5-b]pyridin-2-yl]amino]-1-piperidinyl]ethyl]-3-furancarboxamide ethanedioate(1:2); mp. 160.7° C. (compound 142).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943580
Source datasetuspto-grants-1990_07
ORD IDord-9ee049fd0d1d4c99a27f626131de7824
Source noteuspto-grants-1990_07