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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416251Generated: November 4, 2026

Triethylamine → HCID 15432352, compound

https://huagongshe.com/reaction/1416251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 3345586HCID 3345586—
SolventEthylene GlycolHCID 174—
ProductHCID 15432352HCID 1543235255.3%

Reaction Conditions

Temperature82.5 °C

Reaction Steps

A mixture of 2-(chloromethyl)-6-methylimidazo[1,2-a]pyridine (0.302 g), 1-(4-fluorophenyl) piperazine (Aldrich; 0.319 g), triethylamine (Aldrich; 0.26 mL), and ethylene glycol (2 mL) is stirred for 2.25 h at 80-85° C. The cooled mixture is then poured into saturated aq. sodium bicarbonate and extracted several times with dichloromethane. The combined organic layers are washed with brine, dried with MgSO4, and concentrated under reduced pressure. The crude material is chromatographed on silica gel using methanol/dichloromethane/ammonium hydroxide (4/96/0.25) and crystallized from ethyl acetate/hexane to give 0.300 g of the title compound; mp 112-112.5° C.; ms m/z 324; IR (mineral oil) 1511, 804, 1234, 1246, 1345 cm-1 ; 1H NMR (CDCl3) δ2.31, 2.74, 3.15, 3.76, 6.90, 7.46, 7.86.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912246
Source datasetuspto-grants-1999_06
ORD IDord-8f5f0269353e442680b06f1910ebf735
Source noteuspto-grants-1999_06