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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186794Generated: 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/2186794

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 984608563.5%

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]thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407121B1
Source datasetuspto-grants-2002_06
ORD IDord-63c9ebc6eee64df3ac3666202a4014a1
Source noteuspto-grants-2002_06