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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234470생성일: 2026년 10월 25일

2-Methyl-4-methoxyaniline → N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(4-methoxy-2-methylphenyl)aminocarbonyl]thiophene-3-sulfonamide

https://huagongshe.com/reaction/234470

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-4-methoxyanilineHCID 7610—
반응물N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(2-methyl-1,3,4-thiadiazol-5-yl)aminocarbonyl]thiophene-3-sulfonamideHCID 10550033—
용매PyridineHCID 1049—
생성물N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(4-methoxy-2-methylphenyl)aminocarbonyl]thiophene-3-sulfonamideHCID 10646831—

반응 단계

N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(4-methoxy-2-methylphenyl)aminocarbonyl]thiophene-3-sulfonamide was prepared by the method set forth for N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(2-methyl-1,3,4-thiadiazol-5-yl)aminocarbonyl]thiophene-3-sulfonamide (EXAMPLE 150), except that 4-methoxy-2-methylaniline was used instead of 2-amino-5-methyl-1,3,4-thiadiazole and that pyridine was not used. The title compound was obtained via HPLC purification as a dull yellow powder (66% yield, m.p. 58°-62° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05594021
출처 데이터셋uspto-grants-1997_01
ORD IDord-2858442a5b47413790fae53e184b0f05
출처 메모uspto-grants-1997_01