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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1198688생성일: 2026년 10월 27일

[2'-(N-t-Butylsulfamoyl)biphenyl-4-yl]methyl bromide → 2-(2-Bromo-5-nitrophenyl)-4-[[2'-(N-t-butylsulfamoyl)biphenyl-4-yl]methyl]-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/1198688

반응식

참여 물질

역할이름HCID투입량
반응물[2'-(N-t-Butylsulfamoyl)biphenyl-4-yl]methyl bromideHCID 15282100—
반응물2-(2-Bromo-5-nitrophenyl)-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 135720080—
생성물2-(2-Bromo-5-nitrophenyl)-4-[[2'-(N-t-butylsulfamoyl)biphenyl-4-yl]methyl]-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 1007791792%

반응 단계

The alkylation of 2-(2-bromo-5-nitrophenyl)-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-one (from Step A) with [2'-(N-t-butylsulfamoyl)biphenyl-4-yl]methyl bromide (from Example 7) was carried out according to the procedure of Example 8, Step A, to give a 92% yield of the title compound as a yellow solid, mp 126°-128° C.; homogeneous by TLC in 98:2 CH2Cl2 --MeOH; mass spectrum (FAB) m/e 642, 644 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05281614
출처 데이터셋uspto-grants-1994_01
ORD IDord-d629c9888b564344abbb34e62ef5d050
출처 메모uspto-grants-1994_01