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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684936Generated: October 25, 2026

N,N-Dimethylglycine → Methyl 3-(6-aminopyridin-3-yloxy)benzoate

https://huagongshe.com/reaction/1684936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
ReactantCesium carbonateHCID 10796—
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantMethyl 3-HydroxybenzoateHCID 88068—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 3-(6-aminopyridin-3-yloxy)benzoateHCID 6726326351.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

A procedure described by D. Ma and Q. Cai (Org. Lett. 3799, 2003) was followed. To a solution of 5-bromopyridin-2-amine (346 mg, 2 mmol) in dioxane (10 mL) were added methyl 3-hydroxybenzoate (400 mg, 2.6 mmol), CuI (50 mg), N,N-dimethylglycine (60 mg) and Cs2CO3 (1.0 g). The resulting mixture was heated to 120° C. for 5 h, then cooled and partitioned between water and dichloromethane. The organic layer was separated, dried, and concentrated. The residue was purified by silica gel column eluting with ethyl acetate in dichloromethane (1:1) to obtain methyl 3-(6-aminopyridin-3-yloxy)benzoate (250 mg, 50%) as an oil. LC/MS; (M+H)+=245.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148361B2
Source datasetuspto-grants-2012_04
ORD IDord-1a2cae8af1bd4feda962544efec2b2ed
Source noteuspto-grants-2012_04