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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979909Generated: October 28, 2026

Sulfur → ethyl 4-[[3-(2-furanylmethyl)-3H-imidazo[4,5-b]pyridine-2-yl]amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/979909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfurHCID 5362487—
ReactantEthyl 4-[[[2-[(2-furanylmethyl)amino]-3-pyridinyl]aminothioxomethyl]amino]-1-piperidinecarboxylateHCID 13587973—
CatalystMercuric oxideHCID 30856—
SolventEthanolHCID 702—
Productethyl 4-[[3-(2-furanylmethyl)-3H-imidazo[4,5-b]pyridine-2-yl]amino]-1-piperidinecarboxylateHCID 1358798079%

Reaction Steps

A mixture of 74 parts of ethyl 4-[[[2-[(2-furanylmethyl)amino]-3-pyridinyl]aminothioxomethyl]amino]-1-piperidinecarboxylate, 96 parts of mercury(II)oxide, 0.1 parts of sulfur and 800 parts of ethanol was stirred and refluxed for 3 hours. The reaction mixture was filtered over Hyflo and the filtrate was evaporated. The residue was crystallized from acetonitrile, yielding 52.5 parts (79%) of ethyl 4-[[3-(2-furanylmethyl)-3H-imidazo[4,5-b]pyridin-2-yl]amino]-1-piperidinecarboxylate; mp. 149.2° C. (42).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04634704
Source datasetuspto-grants-1987_01
ORD IDord-2f5e6d6f0fdc4dbda3ba3f2b208c5884
Source noteuspto-grants-1987_01