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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449693Generated: October 25, 2026

Cesium carbonate → Tert-butyl 4-(6-(6-chloro-2-methyl-3-oxo-2,3-dihydropyridazin-4-ylamino)pyridin-3-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/449693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactanttert-Butyl 4-(6-aminopyridin-3-yl)piperidine-1-carboxylateHCID 49839963—
Reactant4-Bromo-6-chloro-2-methyl-2,3-dihydropyridazin-3-oneHCID 59216474—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 4-(6-(6-chloro-2-methyl-3-oxo-2,3-dihydropyridazin-4-ylamino)pyridin-3-yl)piperidine-1-carboxylateHCID 6674224771.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 4-bromo-6-chloro-2-methylpyridazin-3(2H)-one (2.42 g, 10.8 mmol), tert-butyl 4-(6-aminopyridin-3-yl)piperidine-1-carboxylate (2.73 mg, 9.83 mmol), Xantphos (853 mg, 1.47 mmol) and cesium carbonate (9.61 g, 29.5 mmol) in dry dioxane (80 ml) was vacuum de-gassed and place under an argon atmosphere. To this mixture was added tris(dibenzylideneacetone)dipalladium (0) (203 mg, 197 mmol) and the vacuum de-gas cycle was repeated. The material was heated at 90° C. (oil bath) with vigorous stirring overnight. The flask was cooled to ambient temperature and the contents were filtered through a plug of celite, rinsing well with dioxane, the filtrate concentrated and the resulting residue triturated with 1; 1 ratio of ether/ethyl acetate. This provided the desired product as an off-white powder (2.73 g, 71.2%). (M+H)+=420.2 m/e.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481540B2
Source datasetuspto-grants-2013_07
ORD IDord-97b4d57bb8ce4a3aa4975ff315c9f7d9
Source noteuspto-grants-2013_07