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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393177Generated: October 31, 2026

Methanol → 2-amino-4-(4-fluorophenyl)-5-[2-[4-(5-fluoro-1H-benzotriazol-1-yl)piperidin-1-yl]ethyl]thiazole

https://huagongshe.com/reaction/393177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(5-fluoro-1H-benzotriazol-1-yl)piperidineHCID 15462772—
Reactant2-Amino-5-(2-bromoethyl)-4-(4-fluorophenyl)thiazole hydrobromideHCID 22649338—
SolventEthanolHCID 702—
Product2-amino-4-(4-fluorophenyl)-5-[2-[4-(5-fluoro-1H-benzotriazol-1-yl)piperidin-1-yl]ethyl]thiazoleHCID 9846085—

Reaction Steps

A mixture of 0.917 g of 2-amino-5-(2-bromoethyl)-4-(4-fluorophenyl)thiazole hydrobromide, 0.441 g of 4-(5-fluoro-1H-benzotriazol-1-yl)piperidine, 1 ml of diisopropylethylamine and 4 ml of methanol was stirred with heating under reflux for 12 hours. After the reaction mixture was cooled to room temperature, ethanol was added thereto and the crystals were collected by filtration. The crystals were recrystallized from chloroform-ethanol to obtain 0.56 g of 2-amino-4-(4-fluorophenyl)-5-[2-[4-(5-fluoro-1H-benzotriazol-1-yl)piperidin-1-yl]ethyl]thizole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806275B2
Source datasetuspto-grants-2004_10
ORD IDord-a2e92e5d24d7477d9745b792cb1381c5
Source noteuspto-grants-2004_10