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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1247782Erstellt: 26. Oktober 2026

Diisopropylethylamine → 5-Amino-4-[3-(tert-butoxycarbonylamino)propionyl]amino-1-(2-hydroxyethyl)pyrazole

https://huagongshe.com/reaction/1247782

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktSodium BicarbonateHCID 516892—
EduktBoc-Beta-Ala-OSuHCID 10684599—
Edukt4,5-Diamino-1-(2-hydroxyethyl)pyrazole sulfateHCID 11673148—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt5-Amino-4-[3-(tert-butoxycarbonylamino)propionyl]amino-1-(2-hydroxyethyl)pyrazoleHCID 2190446365,5%

Reaktionsschritte

To a suspension of 4,5-diamino-1-(2-hydroxyethyl)pyrazole sulfuric acid salt (2.4 g) in methylene chloride (40 ml) were added N-ethyldiisopropylamine (2.1ml) and N-[3-(tert-butoxycarbonylamino)propionyloxy]succinimide (2.3 g) under ice-cooling, and the mixture was stirred at room temperature for 6 hours. To the reaction mixture were added brine (40 ml) and saturated aqueous sodium hydrogen carbonate solution (20 ml), and the mixture was extracted with a mixture of ethyl acetate and 2-propanol, (3:1, 60 ml). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was triturated with diethyl ether to give 5-amino-4-[3-(tert-butoxycarbonylamino)propionyl]amino-1-(2-hydroxyethyl)pyrazole (1.65 g) as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07129232B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-5cc67e9a7c17493e91fff3aad5122c36
Quellennotizuspto-grants-2006_10