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HRID 50427作成日:2026年10月25日

Naphthalenesulfonamide → 2-ethyl-5,7-dimethyl-3-{4-[2-({[(1-naphthylsulfonyl)amino]carbonyl}amino)ethyl]phenyl}-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/50427

反応式

関与物質

役割名称HCID仕込み量
反応物NaphthalenesulfonamideHCID 163571—
反応物3-{4-[2-({[(4-biphenylsulfonyl)amino]carbonyl}amino)ethyl]phenyl}-2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridineHCID 21875619—
生成物2-ethyl-5,7-dimethyl-3-{4-[2-({[(1-naphthylsulfonyl)amino]carbonyl}amino)ethyl]phenyl}-3H-imidazo[4,5-b]pyridineHCID 21875982—

反応手順

The title compound was prepared according to the procedure described in step 2 of Example 18 from phenyl 2-[4-(2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridin-3-yl)phenyl]ethylcarbamate (step 1 of Example 18) and 1-naphtylsulfonamide (Arnswald, M.; Neumann, W. P. Chem. Ber., 1991, 124, 1997; Khorgami, M. H. Synthesis, 1972, 574).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710054B2
出典データセットuspto-grants-2004_03
ORD IDord-a7d2b85622224ebf95f709ab570bc5cc
出典メモuspto-grants-2004_03