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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1185444Erstellt: 26. Oktober 2026

1-Piperazinecarboxylic acid, ethyl ester → 4-((S)-2-benzyloxycarbonylamino-3-tert-butoxycarbonyl-propionyl)-piperazine-1-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1185444

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Piperazinecarboxylic acid, ethyl esterHCID 8431—
Edukt4-tert-Butyl hydrogen N-((phenylmethoxy)carbonyl)-L-aspartateHCID 111082—
EduktSodium BicarbonateHCID 516892—
EduktO-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733286—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-((S)-2-benzyloxycarbonylamino-3-tert-butoxycarbonyl-propionyl)-piperazine-1-carboxylic acid ethyl esterHCID 66920269—

Reaktionsschritte

To a solution of 25 g of (S)-2-Benzyloxycarbonylamino-succinic acid 4-tert-butyl ester, 35.6 g of NEM and 25.3 g of TOTU in 125 ml of DMF, 12.9 g of Piperazine-1-carboxylic acid ethyl ester was added at RT and stirred for 3 h. The reaction mixture was diluted saturated aqueous sodium hydrogen carbonate solution and extracted with 400 ml of ethyl acetate. The organic phase was washed with diluted saturated aqueous sodium hydrogen carbonate solution and dried over MgSO4 and the solvents were removed under reduced pressure. The crude product was purified by chromatography on silica gel eluting with n-heptane/ethyl acetate (1/1). The fractions containing the product were combined and the solvent evaporated under reduced pressure. Yield: 35.4 g.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08669266B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-a353c04b1cfd4b909f7c6f2e9469fe64
Quellennotizuspto-grants-2014_03