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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085870Generated: November 1, 2026

Carbon Disulfide → 3-(2-ethoxyethyl)-2-[[4-(2-isothiocyanatoethyl)-1-piperazinyl]methyl]-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/1085870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
Reactant4-[[3-(2-ethoxyethyl)-3H-imidazo[4,5-b]pyridin-2-yl]methyl]-1-piperazineethanamineHCID 19911515—
SolventTetrahydrofuranHCID 8028—
Product3-(2-ethoxyethyl)-2-[[4-(2-isothiocyanatoethyl)-1-piperazinyl]methyl]-3H-imidazo[4,5-b]pyridineHCID 19911490100%

Reaction Steps

To a stirred and cooled (-10° C.) mixture of 18 parts of carbon disulfide, 7.22 parts of N,N'-methanetetraylbis[cyclohexanamine] and 135 parts of tetrahydrofuran was added dropwise a solution of 12.9 parts of 4-[[3-(2-ethoxyethyl)-3H-imidazo[4,5-b]pyridin-2-yl]methyl]-1-piperazineethanamine in tetrahydrofuran. Upon complete addition, the temperature was allowed to reach room temperature. After stirring for 1 hour at room temperature, the mixture was evaporated, yielding 13.1 parts (100%) of 3-(2-ethoxyethyl)-2-[[4-(2-isothiocyanatoethyl) -1-piperazinyl]methyl]-3H-imidazo[4,5-b]pyridine as a residue (compound 121)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011842
Source datasetuspto-grants-1991_04
ORD IDord-b3805661d1734cb1b6b515f7c275c9fb
Source noteuspto-grants-1991_04