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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882251Generated: November 2, 2026

2-Amino-3-bromo-5-methylpyridine → 3-bromo-N-(5-chloro-2-((1-methylpiperidin-4-yl)methoxy)phenyl)-5-methylpyridin-2-amine

https://huagongshe.com/reaction/1882251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-3-bromo-5-methylpyridineHCID 519380—
Reactant4-((4-Chloro-2-iodophenoxy)methyl)-1-methylpiperidineHCID 58880166—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
Product3-bromo-N-(5-chloro-2-((1-methylpiperidin-4-yl)methoxy)phenyl)-5-methylpyridin-2-amineHCID 5888015280%

Reaction Steps

In a oven dried 50 mL round bottom flask were sequentially added Compound 173 (620 mg, 1.69 mmol), 3-bromo-5-methylpyridin-2-amine (381 mg, 2.03 mmol), Pd2(dba)3 (77 mg, 0.08 mmol), xantphos (59 mg, 0.10 mmol) and NatBuO (244 mg, 2.53 mmol) at room temperature. The solid materials were kept under vacuum for 5 min. and then refilled with nitrogen. This process was repeated thrice before adding dry, degassed dioxane (8 mL). The heterogeneous mixture was stirred at room temperature for 15 min. and then at 100° C. for 2 h. Finally upon completion of the reaction, it was diluted with EtOAc and filtered through a small pad of silica gel with several washings. All the washings and filtrate concentrated in vacuum and the crude residue was further purified by flash chromatography to provide pure Compound 174 (574 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318939B2
Source datasetuspto-grants-2012_11
ORD IDord-872b6855c77b4d1ab8c445bb2cb64329
Source noteuspto-grants-2012_11