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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36238생성일: 2026년 10월 24일

p-(Methylsulphonyl)benzoic acid → 5-n-Butyl-2,4-dihydro-4-[[2'-[N-[p-(methylsulfonyl)benzoyl]sulfamoyl]-biphenyl-4-yl]methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-one

https://huagongshe.com/ko/reaction/36238

반응식

참여 물질

역할이름HCID투입량
반응물p-(Methylsulphonyl)benzoic acidHCID 77670—
반응물5-n-Butyl-2,4-dihydro-4-[(2'-sulfamoylbiphenyl-4-yl)methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-oneHCID 10346902—
생성물5-n-Butyl-2,4-dihydro-4-[[2'-[N-[p-(methylsulfonyl)benzoyl]sulfamoyl]-biphenyl-4-yl]methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-oneHCID 1993938860%

반응 단계

The title compound was prepared from 5-n-butyl-2,4-dihydro-4-[(2'-sulfamoylbiphenyl-4-yl)methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-one (from Example 16, Step C), according to the procedure of Example 43 except that p-(methylsulfonyl)benzoic acid was used as the acid. The crude product was purified by flash chromatography (gradient elution using 0.5-10% MeOH/CH2Cl2) to afford a 60% yield of the desired compound as a white solid, homogeneous by TLC in 5% MeOH/CH2Cl2 ; mass spectrum (FAB) m/e 735 (M+Na)+, 751 (M+K)+ ; mp 131°-133° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05411980
출처 데이터셋uspto-grants-1995_05
ORD IDord-bb129c8ee71f47c58862a26c4ee156ff
출처 메모uspto-grants-1995_05