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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256649Generated: October 30, 2026

Ethyl 4-[[[[4-[(2-furanylmethyl)amino]-5-pyrimidinyl]amino]thioxomethyl]-amino]-1-piperidinecarboxylate → ethyl 4-[[9-(2-furanylmethyl)-9H-purin-8-yl]amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/256649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-[[[[4-[(2-furanylmethyl)amino]-5-pyrimidinyl]amino]thioxomethyl]-amino]-1-piperidinecarboxylateHCID 19785223—
CatalystMercuric oxideHCID 30856—
SolventEthanolHCID 702—
Productethyl 4-[[9-(2-furanylmethyl)-9H-purin-8-yl]amino]-1-piperidinecarboxylateHCID 1978534121.5%

Reaction Steps

A mixture of 4 parts of ethyl 4-[[[[4-[(2-furanylmethyl)amino]-5-pyrimidinyl]amino]thioxomethyl]-amino]-1-piperidinecarboxylate, 6 parts of mercury(II)oxide and 80 parts of ethanol was stirred for 2 hours at reflux temperature. The whole was filtered while hot over Hyflo® and the filtrate was evaporated. The residue was crystallized from a mixture of acetonitrile and ethanol. The product was filtered off and dried, yielding 0.8 parts (21.5%) of ethyl 4-[[9-(2-furanylmethyl)-9H-purin-8-yl]amino]-1-piperidinecarboxylate; mp. 171.9° C. (compound 7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258380
Source datasetuspto-grants-1993_11
ORD IDord-4e51488da485456c8ba79e6fcfc9b6e1
Source noteuspto-grants-1993_11