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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230092Generated: October 26, 2026

4-Pyridinemethanamine → 6,7-Dimethoxy-4-{4-[2-nitro-1-(4-pyridylmethylamino)vinyl]-1-piperazinyl}quinazoline

https://huagongshe.com/reaction/2230092

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinemethanamineHCID 77317—
Reactant6,7-Dimethoxy-4-[4-(1-methylthio-2-nitrovinyl)-1-piperazinyl]quinazolineHCID 70154916—
SolventPyridineHCID 1049—
Product6,7-Dimethoxy-4-{4-[2-nitro-1-(4-pyridylmethylamino)vinyl]-1-piperazinyl}quinazolineHCID 7015527315.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a pyridine solution (10 mL) of Compound 58 produced in Example 58 (730 mg, 1.87 mmol), 4-aminomethylpyridine (0.57 mL, 5.61 mmol) was added, followed by stirring in argon atmosphere under heating at 80° C. for 5 hours. After the reaction solution was allowed to stand for cooling, the solvent was evaporated, and the resulting residue was purified by silica gel column chromatography to give the target compound (130 mg, 0.29 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423716B1
Source datasetuspto-grants-2002_07
ORD IDord-fa23113b099d493c89eb601015ca31e3
Source noteuspto-grants-2002_07