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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427123Generated: November 4, 2026

Cesium carbonate → Methyl 3-[[6-(4-hydroxy-4-methyl-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoate

https://huagongshe.com/reaction/1427123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactant4-Methylpiperidin-4-olHCID 15649174—
ReactantMethyl 3-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-2,4-dimethyl-benzoateHCID 86707343—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 3-[[6-(4-hydroxy-4-methyl-1-piperidyl)-3-methyl-pyridine-2-carbonyl]amino]-2,4-dimethyl-benzoateHCID 8670735469.3%

Reaction Steps

To a solution of methyl 3-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-2,4-dimethyl-benzoate (315 mg, 946.55 μmoles), 4-methylpiperidin-4-ol (130 mg, 1.13 mmol) and Cs2CO3 (0.9 g, 2.76 mmol) in 1,4-dioxane (7 ml) is added Pd(OAc)2 (25 mg, 89.93 μmoles) followed by racemic-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (56 mg, 89.93 μmoles). The reaction mixture is purged with nitrogen for 5 minutes and then heated to reflux. After 2 hours, the reaction is cooled to ambient temperature and diluted with ammonium chloride and extracted with EtOAc. The combined organic layers are dried over sodium sulfate, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (silica gel) using 0-100% ethyl acetate in hexane to afford the title compound as a brown solid (0.27 g, 69%). Mass spectrum (m/z): 412.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933098B2
Source datasetuspto-grants-2015_01
ORD IDord-534d0f8d9fea44018ae8e50d39cb248c
Source noteuspto-grants-2015_01