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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1655117Erstellt: 25. Oktober 2026

Trityl chloride → methyl (+)-2-n-butyl-5-ethoxycarbonylacetyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate

https://huagongshe.com/reaction/1655117

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrityl chlorideHCID 6456—
EduktTriethylamineHCID 8471—
EduktHCID 178441548HCID 178441548—
LösungsmittelChloroformHCID 6212—
Produktmethyl (+)-2-n-butyl-5-ethoxycarbonylacetyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylateHCID 2007681145,6%

Reaktionsschritte

To a mixture of methyl 2-n-butyl-5-ethoxycarbonylacetyl-3-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (2.0 g), triethylamine (0.69 g) and chloroform (20 ml) is added trityl chloride (1.43 g), and the mixture is stirred at room temperature for 30 minutes. The reaction solution is washed, dried, and evaporated under reduced pressure. The resulting residue is purified by silica gel column chromatography (solvent; ethyl acetate/n-hexane) to give methyl 2-n-butyl-5-ethoxycarbonylacetyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (1.29 g) as needles. m.p. 124°-126° C. (decomposed)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05409936
Quelldatensatzuspto-grants-1995_04
ORD IDord-96b540592d774fa48f70afebb83f1bcc
Quellennotizuspto-grants-1995_04