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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1684936Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1684936

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-DimethylglycineHCID 673—
EduktCesium carbonateHCID 10796—
Edukt2-Amino-5-bromopyridineHCID 70622—
EduktMethyl 3-HydroxybenzoateHCID 88068—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktMethyl 3-(6-aminopyridin-3-yloxy)benzoateHCID 6726326351,2%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08148361B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-1a2cae8af1bd4feda962544efec2b2ed
Quellennotizuspto-grants-2012_04