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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209273Generated: November 1, 2026

Diisopropylethylamine → HCID 57106292, compound

https://huagongshe.com/reaction/2209273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3-Chloro-6-iodopyridazineHCID 15418839—
Solventtert-ButanolHCID 6386—
ProductHCID 57106292HCID 57106292—

Reaction Conditions

Temperature100 °C

Reaction Steps

3-chloro-6-iodopyridazine (510 mg, 2.1 mmol) and tert-butyl piperazine-1-carboxylate (415 mg, 2.23 mmol) were taken up in tBuOH (8 mL). iPr2NEt (480 μL, 2.8 mmol) was added and the stirred reaction mixture was heated to 100° C. After 48 h, the reaction mixture was cooled and was partitioned between EtOAc and water. The phases were separated, and the organic phase was dried over Na2SO4, filtered, and concentrated. The crude residue was purified by silica gel chromatography (0-25% Et2O in DCM) to afford tert-butyl 4-(6-iodopyridazin-3-yl)piperazine-1-carboxylate 7.12. LCMS-ESI+ (m/z): [M+H—CO2tBu]+ calcd for C8H121 N4: 291.0; found: 291.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376441B2
Source datasetuspto-grants-2016_06
ORD IDord-ca82a9e9fe9040549862b21638b5b72f
Source noteuspto-grants-2016_06