Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431137Generated: November 3, 2026

Cesium carbonate → 6-Chloro-4-[6-(2-dimethylamino-1,1-dimethyl-ethoxy)-pyridazin-3-ylamino]-2-methyl-2H-pyridazin-3-one

https://huagongshe.com/reaction/1431137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant4-Bromo-6-chloro-2-methyl-2,3-dihydropyridazin-3-oneHCID 59216474—
Reactant6-(2-Dimethylamino-1,1-dimethyl-ethoxy)-pyridazin-3-ylamineHCID 66742924—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
Solvent1,4-DioxaneHCID 31275—
Product6-Chloro-4-[6-(2-dimethylamino-1,1-dimethyl-ethoxy)-pyridazin-3-ylamino]-2-methyl-2H-pyridazin-3-oneHCID 6674291170.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

In a 15 mL microwave reaction vial was added a solution of 6-(1-(dimethylamino)-2-methylpropan-2-yloxy)pyridazin-3-amine (110 mg, 523 μmol, Eq: 1.00) in dioxane (5 ml) under argon. To the solution was added 4-bromo-6-chloro-2-methylpyridazin-3(2H)-one (152 mg, 680 μmol, Eq: 1.3), Cs2CO3 (511 mg, 1.57 mmol, Eq: 3), xantphos (45.4 mg, 78.5 μmol, Eq: 0.15) and bis(dibenzylideneacetone)palladium (22.6 mg, 39.2 μmol, Eq: 0.075). The reaction tube was sealed and heated in oil bath at 110° C. (bath temp) for 7 hrs, then was cooled to room temperature and stirred overnight. The reaction mixture was filtered and the solid was washed with THF (20 mL). The combined filtrate and washes were concentrated in vacuo. The reaction mixture was absorbed on to silica and purified by LC chromatography eluting with 0-5% (MeOH) in 1/1 EtOAc/heptane to afford 130 mg (70%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940741B2
Source datasetuspto-grants-2015_01
ORD IDord-9f3976cef32a438791744cb9c30c191c
Source noteuspto-grants-2015_01