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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1258387생성일: 2026년 10월 26일

N-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide → N-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide

https://huagongshe.com/reaction/1258387

반응식

참여 물질

역할이름HCID투입량
반응물N-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamideHCID 67329899—
반응물HCID 178527894HCID 178527894—
생성물N-(3-(1H-1,2,4-triazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamideHCID 7728365—
생성물N-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamideHCID 6732989996.5%

반응 단계

N-(3-(1H-1,2,4-triazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide (13e) was prepared according to the procedure for 13d except using 3-mercapto-1,2,4-triazole, which afforded the title compound 38.8 mg (96.5%) as an orange-red solid, m.p.: 197° C. (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08466157B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-88a1511c03c04aad8241a44ae4af647f
출처 메모uspto-grants-2013_06