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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248829Generated: October 25, 2026

3,4-Diaminopyridine → N-(4-amino-3-pyridinyl)-N'-[2-[4-[[9-[(4-fluorophenyl)methyl]-9H-purin-8-yl]amino]-1-piperidinyl]ethyl]thiourea

https://huagongshe.com/reaction/2248829

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DiaminopyridineHCID 5918—
Reactant9-[(4-fluorophenyl)methyl]-N-[1-(2-isothiocyanatoethyl)-4-piperidinyl]-9H-purin-8-amineHCID 19785225—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-amino-3-pyridinyl)-N'-[2-[4-[[9-[(4-fluorophenyl)methyl]-9H-purin-8-yl]amino]-1-piperidinyl]ethyl]thioureaHCID 19785224—

Reaction Steps

A mixture of 2.95 parts of 3,4-pyridinediamine, 16 parts of 9-[(4-fluorophenyl)methyl]-N-[1-(2-isothiocyanatoethyl)-4-piperidinyl]-9H-purin-8-amine, and 90 parts of tetrahydrofuran was stirred and refluxed overnight. The reaction mixture was evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (95/5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 10.5 parts of N-(4-amino-3-pyridinyl)-N'-[2-[4-[[9-[(4-fluorophenyl)methyl]-9H-purin-8-yl]amino]-1-piperidinyl]ethyl]thiourea (compound 182).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041448
Source datasetuspto-grants-1991_08
ORD IDord-b4418bdf11744bf59a2eda7c09c68bf6
Source noteuspto-grants-1991_08