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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1166985생성일: 2026년 10월 26일

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/1166985

반응식

참여 물질

역할이름HCID투입량
반응물1-(6-Amino-1,3-benzodioxol-5-yl)ethan-1-oneHCID 120000—
반응물2-Amino-4,5-dimethoxybenzonitrileHCID 735967—
반응물N-(4-chloro-3-methyl-5-isoxazolyl)2-{[2-acetyl-4,5-(methylenedioxy)phenyl]aminocarbonyl}thiophene-3-sulfonamideHCID 10696210—
생성물N-(4-chloro-3-methyl-5-isoxazolyl)-2-[{2-cyano-4, 5-dimethoxyphenyl)aminocarbonyl]-thiophene-3-sulfonamideHCID 9956918—

반응 단계

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.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06613804B2
출처 데이터셋uspto-grants-2003_09
ORD IDord-407fc3adef764ed489d6bef04350f8c9
출처 메모uspto-grants-2003_09