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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336528Erstellt: 25. Oktober 2026

Diisopropylethylamine → HCID 68000123, Verbindung

https://huagongshe.com/reaction/336528

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt4-Nitrophenyl chloroformateHCID 82129—
EduktEthyl 5-(hydroxymethyl)isoxazole-3-carboxylateHCID 8027233—
Edukttert-Butyl 2-amino-6-azaspiro[3.4]octane-6-carboxylateHCID 56962195—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelWaterHCID 962—
ProduktHCID 68000123HCID 6800012373,9%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of 0.304 g (1.51 mmol) of 4-nitrophenyl chloroformate dissolved in 5 mL of 1,2-dichloroethane is added dropwise to a solution containing 0.284 g (1.66 mmol) of ethyl 5-hydroxymethylisoxazole-3-carboxylate and 0.39 g (3.02 mmol) of N,N-diisopropylethylamine in 10 mL of 1,2-dichloroethane, cooled to about 0° C. Stirring is continued at 0° C. for 1 hour and then at room temperature for 1 hour. 0.39 g (3.02 mmol) of N,N-diisopropylethylamine and then 0.34 g (1.51 mmol) of tert-butyl 2-amino-6-azaspiro[3.4]octane-6-carboxylate, prepared in step 6.4., are added. The reaction medium is stirred at 70° C. for 4 hours. It is allowed to cool to room temperature. Water is added to the reaction medium, the aqueous phase is separated out and extracted several times with dichloromethane, the combined organic phases are washed with aqueous sodium hydroxide solution (1N) and then with saturated aqueous ammonium chloride solution and dried over sodium sulfate, and the filtrate is concentrated under reduced pressure. 0.44 g of pure product is thus obtained in the form of an orange oil, which is used without further purification in the following step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889702B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-c3524bda5e0d4f5b8b9a9cb08c4392a6
Quellennotizuspto-grants-2014_11