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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630458Generated: October 30, 2026

Diisopropylethylamine → HCID 59242666, compound

https://huagongshe.com/reaction/1630458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant6-Chloro-4-phenyl-3-(trifluoromethyl)pyridazineHCID 59242649—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 59242666HCID 5924266693%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a stirred solution of 6-chloro-4-phenyl-3-trifluoromethyl-pyridazine (D3) (7.1 g, 0.0274 mol) and N-Boc-piperazine (5.62 g, 0.0302 mol) in acetonitrile (150 ml) was added diisopropylethylamine (5.1 ml, 0.0302 mol) and the mixture heated at 150° C. for 20 min., under microwave irradiation. After this period, the reaction mixture was diluted with dichloromethane and extracted with water. The organic layer was separated, dried (MgSO4) and the solvents evaporated in vacuo. The crude product was purified by column chromatography (silica; 20% ethyl acetate in heptane, followed by 10% ethyl acetate in dichloromethane). After evaporation of the solvent, the crude product was crystallised from heptane to yield D4 (10.4 g, 93%). C20H23F3N4O2 requires 408; Found 409 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791120B2
Source datasetuspto-grants-2014_07
ORD IDord-bf0795a049ec4fb7bfdb7e65a9d55a94
Source noteuspto-grants-2014_07