Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264874Generated: October 31, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 5-Amino-2-(2-furyl)-7-(4-(2-hydroxy-2-methylpropyl)piperazinyl)[1,2,4]triazolo[1,5-c]pyrimidine

https://huagongshe.com/reaction/1264874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Methyl-1-(piperazin-1-yl)propan-2-olHCID 258202—
Reactant5-Amino-7-chloro-2-(2-furyl)[1,2,4]triazolo[1,5-c]pyrimidineHCID 9942767—
SolventDimethyl SulfoxideHCID 679—
Product5-Amino-2-(2-furyl)-7-(4-(2-hydroxy-2-methylpropyl)piperazinyl)[1,2,4]triazolo[1,5-c]pyrimidineHCID 1548918533%

Reaction Conditions

Temperature140 °C

Reaction Steps

Into 7 mL of DMSO, 500 mg (2.12 mmol) of Compound E was dissolved, and then 0.95 mL (6.36 mmol) of DBU and 1.50 g (9.50 mmol) of 1-(2-hydroxy-2-methylpropyl)piperazine were added thereto, followed by stirring at 140° C. for about 2 hours. After completion of the reaction, the reaction mixture was extracted by adding chloroform and water, and the organic layer was washed with water and brine, and then dried over anhydrous magnesium sulfate. After evaporation of the solvent, the resulting residue was purified by silica gel column chromatography (3% methanol-chloroform) and then recrystallized from a mixed solvent of hexane-ethyl acetate to obtain 250 mg of Compound 1 as a white solid (yield: 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06545000B1
Source datasetuspto-grants-2003_04
ORD IDord-e2148aa9fbf54eeebc9d8a6054e8592c
Source noteuspto-grants-2003_04