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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1861638생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물N-benzyl-4-methoxybenzenesulfonamideHCID 741351—
반응물ethyl 4-chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylateHCID 2736380—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물Ethyl 4-[benzyl-(4-methoxybenzenesulfonyl)amino]-1,3-dimethyl-1H-pyrazolo[3,4-b] pyridine-5-carboxylateHCID 2232211236,901.301%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06534491B2
출처 데이터셋uspto-grants-2003_03
ORD IDord-1dd4719cd0f84e8e984528f455529eca
출처 메모uspto-grants-2003_03