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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36221Erstellt: 24. Oktober 2026

Chloromethyl phenyl sulphide → 5-n-Butyl-2,4-dihydro-2-(phenylthiomethyl)-4-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]-3H-1,2,4-triazol-3-one

https://huagongshe.com/de/reaction/36221

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloromethyl phenyl sulphideHCID 81623—
Edukt5-n-Butyl-2,4-dihydro-4-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]-3H-1,2,4-triazol-3-oneHCID 19939386—
Produkt5-n-Butyl-2,4-dihydro-2-(phenylthiomethyl)-4-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]-3H-1,2,4-triazol-3-oneHCID 1993936417%

Reaktionsschritte

The alkylation of 5-n-butyl-2,4-dihydro-4-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]-3H-1,2,4-triazol-3-one (from Example 2, Step D) with chloromethyl phenyl sulfide was carried out as described in Example 3, Step A, except that only 5 equivalents of the alkylating agent was used. After work-up, the residue was flash chromatographed over silica gel (25 mL for 0.162 mole, gradient elution using 0.25-1.0% MeOH/CH2Cl2) to give the desired material as a colorless oil in 17% yield, homogeneous by TLC in 2% MeOH/CH2Cl2, mass spectrum (FAB) m/e 740 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05411980
Quelldatensatzuspto-grants-1995_05
ORD IDord-b90e735c3fdc4cd9bfb1a63e5732a88a
Quellennotizuspto-grants-1995_05