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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708928Generated: November 1, 2026

Sulfur → HCID 178467910, compound

https://huagongshe.com/reaction/1708928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfurHCID 5362487—
ReactantN-(4-amino-3-pyridinyl)-N'-[2-[4-[[3-(2-ethoxyethyl)-3H-imidazo[4,5-b]pyridin-2-yl]methyl)-1-piperazinyl]ethyl]thioureaHCID 19911578—
CatalystMercuric oxideHCID 30856—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178467910HCID 17846791030%

Reaction Steps

A mixture of 16.9 parts of N-(4-amino-3-pyridinyl)-N'-[2-[4-[[3-(2-ethoxyethyl)-3H-imidazo[4,5-b]pyridin-2-yl]methyl)-1-piperazinyl]ethyl]thiourea, 11.4 parts of mercury(II)oxide, 0.1 parts of sulfur and 135 parts of tetrahydrofuran was stirred for 3 hours at reflux temperature. The reaction mixture was filtered while hot over diatomaceous earth and the filtrate was evaporated. The residue was purified by column chromatography over silica gel using a mixture of dichloromethane and methanol, saturated with ammonia, (90:10 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was stirred in 2,2'-oxybispropane. The product was filtered off and dried, yielding 4.73 parts (30.0%) of N-[2-[4-[[3-(2-ethoxyethyl)-3H-imidazo[4,5-b]pyridin-2-yl]methyl]-1-piperazinyl]ethyl]-1H-imidazo[4,5-c]pyridin-2-amine; mp. 124.5° C. (compound 123).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04946843
Source datasetuspto-grants-1990_08
ORD IDord-8ec942aae0c4409cb31d8d5a1a175b26
Source noteuspto-grants-1990_08