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HRID 1194152Erstellt: 25. Oktober 2026

Potassium Phosphate, Tribasic → 3-(3-methyl-4-methoxyphenyl)methyl-N-BOC-histidine methyl ester

https://huagongshe.com/reaction/1194152

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
EduktDiisopropylethylamineHCID 81531—
EduktMethanesulfonic anhydrideHCID 81560—
EduktN(alpha), N-(im)-Di-Boc-L-histidine methyl esterHCID 10904703—
Edukt(4-Methoxy-3-methylphenyl)methanolHCID 14457544—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(3-methyl-4-methoxyphenyl)methyl-N-BOC-histidine methyl esterHCID 18631280—

Reaktionsbedingungen

Temperatur-25 °C

Reaktionsschritte

A solution of 10.8 g methanesulfonic anhydride in 120 mL dichloromethane is chilled to -50° C. and treated dropwise with a solution of 9.4 g 3-methyl-4-methoxybenzyl alcohol, 10.8 mL diisopropylethylamine and 80 mL dichloromethane. The resulting solution is warmed to -25° C. over 30 min and treated dropwise with 20.0 g N,1-bis-BOC-histidine methyl ester dissolved in 125 mL dichloromethane. The mixture is then allowed to warm to 25° C. over 4 hr, stirring at this temperature 24 hr. The reaction mixture is poured into 700 mL 0.25M, pH=7 potassium phosphate buffer and the organic layer is separated, dried and evaporated. Chromatography on silica gel, eluting with chloroformmethanol (99:1) gives 3-(3-methyl-4-methoxyphenyl)methyl-N-BOC-histidine methyl ester as a gum. NMR (CDCl3) 1.43 (s,9H,t-Bu).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04812462
Quelldatensatzuspto-grants-1989_03
ORD IDord-f659c5288ab54b87980308e431266723
Quellennotizuspto-grants-1989_03