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HRID 36294생성일: 2026년 10월 23일

4-(4-Bromo-2-fluorobenzyl)-5-n-butyl-2-(2-chloro-5-nitrophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-one → 5-n-Butyl-4-[[2'-(N-t-butylsulfamoyl)-3-fluoro-5'-n-propylbiphenyl-4-yl]methyl]-2-(2-chloro-5-nitrophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-one

https://huagongshe.com/ko/reaction/36294

반응식

참여 물질

역할이름HCID투입량
반응물4-(4-Bromo-2-fluorobenzyl)-5-n-butyl-2-(2-chloro-5-nitrophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 19939472—
반응물(2-(N-(tert-Butyl)sulfamoyl)-5-propylphenyl)boronic acidHCID 19939476—
생성물5-n-Butyl-4-[[2'-(N-t-butylsulfamoyl)-3-fluoro-5'-n-propylbiphenyl-4-yl]methyl]-2-(2-chloro-5-nitrophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 1993939043%

반응 단계

Using the method of Example 76, Step F, 4-(4-bromo-2-fluorobenzyl)-5-n-butyl-2-(2-chloro-5-nitrophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-one (from Step A) was coupled with 2-(N-t-butylsulfamoyl)-5-n-propylphenylboronic acid (from Example 68, Step B). Flash chromatography of the crude product on silica gel (gradient elution with 6:1 to 2:1 hexane-EtOAc) gave a 43% yield of the title compound as a cream-colored solid, mp 84°-86° C.; homogeneous by TLC (4:1 hexane-EtOAc).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05411980
출처 데이터셋uspto-grants-1995_05
ORD IDord-c1502034cc6a49d49b7d12eb09a6140b
출처 메모uspto-grants-1995_05