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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36277Erstellt: 24. Oktober 2026

[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/de/reaction/36277

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt[2'-(N-t-Butylsulfamoyl)biphenyl-4-yl]methyl bromideHCID 15282100—
Edukt2-(2-Bromo-5-nitrophenyl)-5-n-butyl-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 135720080—
Produkt2-(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%

Reaktionsschritte

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 12, Step D) was carried out according to the procedure of Example 13, 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)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05411980
Quelldatensatzuspto-grants-1995_05
ORD IDord-efaccb8a782d42b8af7303a45639d2b3
Quellennotizuspto-grants-1995_05