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HRID 926940Erstellt: 26. Oktober 2026

Bicarbonate Ion → (2R)-2-Phenylcarbonyloxypropyl(2S)-2-(tert-Butoxycarbonyl)amino-3-(3,4-dihydroxyphenyl)propanoate

https://huagongshe.com/reaction/926940

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBicarbonate IonHCID 769—
EduktN-methyl-2-pyrrolidoneHCID 13387—
EduktN-(tert-Buloxycarbonyl)-3,4-dihydroxy-L-phenylalanineHCID 14217229—
EduktBoc-L-dopa tetrabutylammonium saltHCID 131728417—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
Produkt(2R)-2-Phenylcarbonyloxypropyl(2S)-2-(tert-Butoxycarbonyl)amino-3-(3,4-dihydroxyphenyl)propanoateHCID 46899463—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Boc-Dopa TBA salt 3 (50 g, 93 mmol), bicarbonate-washed (1R)-2-chloroisopropyl benzoate 5 (20 g, 100 mmol), and N-methylpyrrolidinone (NMP) (100 mL) were added to a 250 mL round bottom flask. The mixture was stirred under a nitrogen atmosphere and heated in an oil bath at 100° C. After ca. 72 hrs the reaction was cooled to room temperature, diluted with tert-butyl methylether (MTBE) (1 L), and washed twice with deionized water (2 L, then 1 L). The organic phase was separated, dried over anhydrous sodium sulfate (Na2SO4), filtered, and concentrated under reduced pressure to provide 35 g (76 mmol) of (2R)-2-phenylcarbonyloxypropyl(2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoate 6 as a tan, viscous oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09290445B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-ac6d7a3090f84f31b3a45f1c609b470a
Quellennotizuspto-grants-2016_03