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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1247798Erstellt: 26. Oktober 2026

N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide ester → 5-Amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole

https://huagongshe.com/reaction/1247798

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
EduktDiisopropylethylamineHCID 81531—
Edukt4,5-Diamino-1-(2-hydroxyethyl)pyrazole sulfateHCID 11673148—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-Amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazoleHCID 2190451580,8%

Reaktionsschritte

To a suspension of 4,5-diamino-1-(2-hydroxyethyl)pyrazole sulfuric acid salt (1.20 g) and N-[2-(tert-butoxycarbonylamino)acetoxy]succinimide (1.35 g) in methylene chloride (20 ml) was added N-ethyldiisopropylamine (2.1 ml) under ice-cooling, and the mixture was stirred at room temperature for 17 hours. The reaction mixture was washed with water (40 ml), saturated aqueous sodium hydrogen carbonate solution (40 ml) and brine (40 ml). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The oily residue was purified by column chromatography on silica gel eluting with 10% methanol/chloroform to give 5-amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole (1.20 g) as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07129232B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-52dd1d3126c343a9b2cb3cf6af9914c6
Quellennotizuspto-grants-2006_10