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HRID 2270745作成日:2026年10月26日

1-(6-Amino-1,3-benzodioxol-5-yl)ethan-1-one → N-(4-chloro-3-methyl-5-isoxazolyl)-2-[{2-cyano-4, 5-dimethoxyphenyl)aminocarbonyl]-thiophene-3-sulfonamide

https://huagongshe.com/reaction/2270745

反応式

関与物質

役割名称HCID仕込み量
反応物1-(6-Amino-1,3-benzodioxol-5-yl)ethan-1-oneHCID 120000—
反応物2-Amino-4,5-dimethoxybenzonitrileHCID 735967—
反応物N-(4-chloro-3-methyl-5-isoxazolyl)2-{[2-acetyl-4,5-(methylenedioxy)phenyl]aminocarbonyl}thiophene-3-sulfonamideHCID 10696210—
生成物N-(4-chloro-3-methyl-5-isoxazolyl)-2-[{2-cyano-4, 5-dimethoxyphenyl)aminocarbonyl]-thiophene-3-sulfonamideHCID 9956918—

反応手順

N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(2-cyano-4,5-dimethoxyphenyl)aminocarbonyl]thiophene-3-sulfonamide was prepared by the method set forth for N-(4-chloro-3-methyl-5-isoxazolyl)2-{[2-acetyl-4,5-(methylenedioxy)phenyl]aminocarbonyl}thiophene-3-sulfonamide (EXAMPLE 148) except that 2-amino-4,5-dimethoxybenzonitrile was used in stead of 2′-amino-4′,5′-(methylenedioxy)acetophenone. N-(4-chloro-3-methyl-5-isoxazolyl)-2-[{2-cyano-4,5-dimethoxyphenyl)aminocarbonyl]-thiophene-3-sulfonamide was obtained via HPLC purification as a light brown powder (36% yield, m.p. 53-56° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06331637B1
出典データセットuspto-grants-2001_12
ORD IDord-c67e94581d28485084abb9a1d8511fec
出典メモuspto-grants-2001_12