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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300246Generated: October 31, 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/2300246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-benzyl-4-methoxybenzenesulfonamideHCID 741351—
Reactantethyl 4-chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylateHCID 2736380—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductEthyl 4-[benzyl-(4-methoxybenzenesulfonyl)amino]-1,3-dimethyl-1H-pyrazolo[3,4-b] pyridine-5-carboxylateHCID 2232211236,901.301%

Reaction Steps

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 170-172°. 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498167B2
Source datasetuspto-grants-2002_12
ORD IDord-fab78ee25da64ad3b86cf510c4d87297
Source noteuspto-grants-2002_12