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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166135Generated: November 3, 2026

Sodium Carbonate → 3-(2-ethoxyethyl)-N-[1-(2-ethoxyethyl)-4-piperidinyl]-3H-imidazo[4,5-b]pyridin-2-amine ethanedioate

https://huagongshe.com/reaction/2166135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantEthane, 1-chloro-2-ethoxy-HCID 12341—
ReactantDimethylacetamideHCID 31374—
Reactant3-(2-ethoxyethyl)-N-(4-piperidinyl)-3H-imidazo[4,5-b]pyridin-2-amineHCID 15718816—
SolventWaterHCID 962—
Product3-(2-ethoxyethyl)-N-[1-(2-ethoxyethyl)-4-piperidinyl]-3H-imidazo[4,5-b]pyridin-2-amine ethanedioateHCID 13171647512.9%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1.08 parts of 1-chloro-2-ethoxyethane, 2.9 parts of 3-(2-ethoxyethyl)-N-(4-piperidinyl)-3H-imidazo[4,5-b]pyridin-2-amine, 1.06 parts of sodium carbonate and 45 parts of N,N-dimethylacetamide was stirred overnight at 70° C. The reaction mixture was poured into water and the product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by filtration 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 methanol. The salt was filtered off and dried, yielding 0.7 parts (12.9%) of 3-(2-ethoxyethyl)-N-[1-(2-ethoxyethyl)-4-piperidinyl]-3H-imidazo[4,5-b]pyridin-2-amine ethanedioate(1:2); mp. 176.1° C. (compound 44).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943580
Source datasetuspto-grants-1990_07
ORD IDord-ca4a2b26daee4154b151275ace681bd8
Source noteuspto-grants-1990_07