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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1861638Erstellt: 26. Oktober 2026

N-benzyl-4-methoxybenzenesulfonamide → Ethyl 4-[benzyl-(4-methoxybenzenesulfonyl)amino]-1,3-dimethyl-1H-pyrazolo[3,4-b] pyridine-5-carboxylate

https://huagongshe.com/reaction/1861638

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-benzyl-4-methoxybenzenesulfonamideHCID 741351—
Eduktethyl 4-chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylateHCID 2736380—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktEthyl 4-[benzyl-(4-methoxybenzenesulfonyl)amino]-1,3-dimethyl-1H-pyrazolo[3,4-b] pyridine-5-carboxylateHCID 2232211236.901,301%

Reaktionsschritte

The mixture was heated in an oil bath at 50° C. overnight and then was heated in an oil bath at 100° C. for 1.5 days. The mixture was poured into 800 ml of water and extracted with ethyl acetate. The extract was washed with water, 2N citric acid, water, brine and dried (Na2SO4). The solvent was removed and the residue chromatographed on silica gel with hexane-ethyl acetate (2:1) as eluent to give 0.64 g of product as a solid, mp 170-1720. From a larger scale run of 5.07 g (0.02 mmol) of ethyl 4-chloro-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxylate and 8.0 g (0.0289 mmol) of benzyl-(4-methoxybenzenesulfonyl) amine (as sodium anion) in 30 ml of 1-methyl-2-pyrrolidinone heated at 90° C. for 3 days there was obtained 3.65 g of product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06534491B2
Quelldatensatzuspto-grants-2003_03
ORD IDord-1dd4719cd0f84e8e984528f455529eca
Quellennotizuspto-grants-2003_03