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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630467Generated: November 1, 2026

Diisopropylethylamine → HCID 59242671, compound

https://huagongshe.com/reaction/1630467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3,6-Dichloro-4-phenylpyridazineHCID 11322080—
SolventAcetonitrileHCID 6342—
ProductHCID 59242671HCID 5924267120.1%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 3,6-dichloro-4-phenyl-pyridazine (0.41 g, 1.82 mmol), prepared by following the procedure described in WO-2005/013907, N-Boc-piperazine (0.509 g, 2.73 mmol) and diisopropylethylamine (0.634 ml, 3.64 mmol) in acetonitrile (7.5 ml) was stirred at 180° C. for 40 min., under microwave irradiation, and then for a further 30 min. After this period, additional amounts of diisopropylethylamine (0.1 ml, 0.57 mmol) and N-Boc-piperazine (0.1 g, 0.54 mmol) were added and the resulting mixture was stirred at 180° C. for 40 min. The solvent was evaporated in vacuo and then, dichloromethane and a saturated solution of ammonium chloride were added. The organic layer was separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The residue was then purified by column chromatography (silica gel; dichloromethane and heptane/ethyl acetate 8:2 to 7:3). The desired fractions were collected and evaporated in vacuo to yield D13 (0.137 g, 20%) as a white solid. C19H23ClN4O2 requires 374; Found 375 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791120B2
Source datasetuspto-grants-2014_07
ORD IDord-0b95c5aa1c5249c1ae5c52b30ea33b00
Source noteuspto-grants-2014_07