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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431107Generated: October 30, 2026

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

https://huagongshe.com/reaction/1431107

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—
ReactantTert-butyl 3-(6-aminopyridin-3-yl)pyrrolidine-1-carboxylateHCID 66742238—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 3-(6-(6-chloro-2-methyl-3-oxo-2,3-dihydropyridazin-4-ylamino)pyridin-3-yl)pyrrolidine-1-carboxylateHCID 6674279050%

Reaction Conditions

Temperature100 °C

Reaction Steps

Tert-butyl 3-(6-aminopyridin-3-yl)pyrrolidine-1-carboxylate (422 mg, 1.6 mmol, Eq: 1.00), 4-bromo-6-chloro-2-methylpyridazin-3(2H)-one (430 mg, 1.92 mmol, Eq: 1.20), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (139 mg, 240 μmol, Eq: 0.15), cesium carbonate (1.57 g, 4.81 mmol, Eq: 3) and tris(dibenzylideneacetone)dipalladium(0) (73.4 mg, 80.1 μmol, Eq: 0.05) were combined in dioxane (10 ml). The solution was degassed with Ar for 10 min. The mixture was heated at 100° C. for 18 h. The solution was cooled to room temperature then diluted with 100 ml DCM. The organics washed with water, then dried over MgSO4. The solution was filtered. Concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 40 g, 50% to 100% EtOAC/Hex gradient) to give tert-butyl 3-(6-(6-chloro-2-methyl-3-oxo-2,3-dihydropyridazin-4-ylamino)pyridin-3-yl)pyrrolidine-1-carboxylate (325 mg, 50%) LC/MS-ESI observed [M+H]+ 406.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940741B2
Source datasetuspto-grants-2015_01
ORD IDord-9f2d504ba05c4e03adda819caa8fb9c3
Source noteuspto-grants-2015_01