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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266320Generated: November 2, 2026

4-Benzylpiperidine → HCID 11993597, compound

https://huagongshe.com/reaction/2266320

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BenzylpiperidineHCID 31738—
ReactantHCID 11993498HCID 11993498—
SolventMethanolHCID 887—
ProductHCID 11993597HCID 1199359766.4%

Reaction Steps

A solution of ethyl 6-(2-chlorophenyl)-7-(4-chlorophenyl)-[1,2,4]triazolo[4,3-b]pyridazine-3-carboxylate (21 mg, 0.05 mmol) and 4-benzylpiperidine (0.175 mL, 1.0 mmol) in methanol (0.5 mL) was heated in a microwave oven at 160° C. for 30 min. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure, then the crude product was purified using reverse phase preparative HPLC (Conditions: Water SunFire Prep C18, OBD 19×100 m, 5 □m; Fluted with 0% to 100% B, 10 min gradient, 100% B hold for 5 min, (A 90% H2O, 10% MeOH, 0.1% of TEA and B 10% H2O, 90% MeOH, 0.1% of TFA); Flow rate at 20 mL/min, UV detection at 220 nm) to afford 18 mg (66%) of the title compound as a white powder. HPLC/MS (method A): retention time=4.12 min, (M+H)+=542.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858639B2
Source datasetuspto-grants-2010_12
ORD IDord-7985d932178a472781c4d0c96d6a1b27
Source noteuspto-grants-2010_12