Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485853Generated: October 31, 2026

Diisopropylethylamine → HCID 59242666, compound

https://huagongshe.com/reaction/1485853

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 numberUS09422296B2
Source datasetuspto-grants-2016_08
ORD IDord-77c3d811a315493ea83f992e39739e7b
Source noteuspto-grants-2016_08