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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630463Generated: October 31, 2026

Diisopropylethylamine → tert-Butyl 4-[6-(trifluoromethyl)pyridazin-3-yl]piperazine-1-carboxylate

https://huagongshe.com/reaction/1630463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3-Chloro-6-(trifluoromethyl)pyridazineHCID 28242526—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 4-[6-(trifluoromethyl)pyridazin-3-yl]piperazine-1-carboxylateHCID 5348551399%

Reaction Steps

A mixture of 6-chloro-3-trifluoromethylpyridazine (0.666 g, 5.09 mmol) (prepared by following the procedure described in Goodman, A. J.; Stanforth, S. P; Tarbit B. Tetrahedron 1999, 55, 15067-15070), N-Boc-piperazine (1.138 g, 6.11 mmol) and diisopropylethylamine (1.95 ml, 1.12 mmol) in acetonitrile (10 ml) was stirred at 180° C. for 30 min., under microwave irradiation. The solvent was evaporated in vacuo and the residue was purified by column chromatography (silica gel; hexane/ethyl acetate) to yield D9 (1.67 g, 99%) as a light yellow solid. C14H19F3N4O2 requires 332; Found 333 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791120B2
Source datasetuspto-grants-2014_07
ORD IDord-70371dca357d49fe9abf6cfc6bd6f45a
Source noteuspto-grants-2014_07