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HRID 1861638作成日:2026年10月25日

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

反応式

関与物質

役割名称HCID仕込み量
反応物N-benzyl-4-methoxybenzenesulfonamideHCID 741351—
反応物ethyl 4-chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylateHCID 2736380—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物Ethyl 4-[benzyl-(4-methoxybenzenesulfonyl)amino]-1,3-dimethyl-1H-pyrazolo[3,4-b] pyridine-5-carboxylateHCID 2232211236,901.301%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06534491B2
出典データセットuspto-grants-2003_03
ORD IDord-1dd4719cd0f84e8e984528f455529eca
出典メモuspto-grants-2003_03