Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581635Generated: November 1, 2026

4-[3-(2-Fluorophenyl)-[1,2,3]triazolo[1,5-a]quinazolin-5-yl]piperazine-1-carboxylic acid tert-butyl ester → 3-(2-Fluorophenyl)-5-(piperazin-1-yl)-[1,2,3]triazolo[1,5-a]quinazoline

https://huagongshe.com/reaction/1581635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[3-(2-Fluorophenyl)-[1,2,3]triazolo[1,5-a]quinazolin-5-yl]piperazine-1-carboxylic acid tert-butyl esterHCID 70031188—
SolventDichloromethaneHCID 6344—
Product3-(2-Fluorophenyl)-5-(piperazin-1-yl)-[1,2,3]triazolo[1,5-a]quinazolineHCID 70032510109.4%

Reaction Steps

4-[3-(2-Fluorophenyl)-[1,2,3]triazolo[1,5-α]quinazolin-5-yl]piperazine-1-carboxylic acid tert-butyl ester (0.28 g, 0.63 mmol) was dissolved in dichloromethane (5 ml) and hydrogen chloride bubbled through the reaction (2×10 min). The precipitate was filtered and washed with diethyl ether to give 3-(2-fluorophenyl)-5-(piperazin-1-yl)-[1,2,3]triazolo[1,5-α]quinazoline as a white solid (0.24 g, 100%). HCl salt: δH (360 MHz; DMSO) 3.30-3.41 (4H, m), 3.79-3.83 (4H, m), 7.35-7.41 (2H, m), 7.44-7.51 (1H, m), 7.78 (1H, ddd, J=8, 8 and 1), 8.05-8.12 (2H, m), 8.27 (1H, d, J=8), 8.62 (1H, dd, J=8 and 1); m/z (ES+) 349 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730681B2
Source datasetuspto-grants-2004_05
ORD IDord-47ee02e20dbd438b9e88f252f64a5ed2
Source noteuspto-grants-2004_05