Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552161Generated: October 30, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 11616280, compound

https://huagongshe.com/reaction/552161

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
Reactant6-chloro-N-(3-methylbutyl)pyridazine-3-carboxamideHCID 16733786—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 11616280HCID 1161628050%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 6-chloropyridazine-3-carboxylic acid (3-methylbutyl)amide (0.140 g, 0.610 mmol) in DMF (7 mL) was added piperidin-4-ylcarbamic acid tert-butyl ester (0.146 g, 0.730 mmol), followed by the addition of 1,8-diazabicyclo[5,4,0]undec-7-ene (0.280 mL, 1.84 mmol) and tetra-n-butylammonium iodide (6 mg). The reaction mixture was stirred at 80° C. for 16 hours. The solvent was removed in vacuo. The residue was dissolved in ethyl acetate, then washed with citric acid, sodium bicarbonate and brine solution. The organic layer was separated, and dried over anhydrous Na2SO4, and evaporated. The residue was purified by column chromatography and then treated with trifluoroacetic acid. The title compound was obtained as a white powder in 50% yield (0.090 g). 1H NMR (300 MHz, DMSO-d6) δ 8.75-8.77 (m, 1H), 7.79 (d, J=9.6 Hz, 1H), 7.34 (d, J=9.6 Hz, 1H), 4.29-4.35 (m, 2H), 3.29-3.22 (m, 1H), 3.06-3.12 (m, 1H), 2.85-2.87 (m, 1H), 2.50 (m, 1H), 1.77-1.80 (m, 2H), 1.56-1.64 (m, 4H), 1.40-1.44 (m, 2H), 1.17-1.25 (m, 1H), 0.90 (d, J=6.6 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951805B2
Source datasetuspto-grants-2011_05
ORD IDord-79b59a3c01974e20ad7f8f7f0f085e49
Source noteuspto-grants-2011_05