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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 645772Erstellt: 23. Oktober 2026

Diisopropylethylamine → HCID 28776588, Verbindung

https://huagongshe.com/de/reaction/645772

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt3,5-Dimethylisoxazole-4-carbonyl ChlorideHCID 2736265—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 28776588HCID 28776588—

Reaktionsschritte

A solution of 1-tert-butyloxycarbonyl-piperazine (4.581 mmol, 0.9 eq) and diisopropylethylamine (5.09 mmol, 1.0 eq) in methylene chloride (5 mL) was added to a 40 mL vial. 3,5-Dimethyl-isoxazole-4-carbonyl chloride (5.09 mmol, 1.0 eq) was added to the vial and the reaction was shaken overnight at room temperature. When the reaction was complete, it was diluted with methylene chloride (5 mL) and washed with 4 mL of 1N hydrochloric acid followed by 4 mL of 10% potassium carbonate. The organic layer was concentrated in vacuo. The crude residue was dissolved in 5 mL of dioxane and 5 mL of 4M hydrochloric acid in dioxane. The reaction mixture was shaken overnight at room temperature then centrifuged. The supernatant was removed and the remaining solid was shaken with hexane then centrifuged. The supernatant was removed, and the solids were collected and dried in vacuo to give (3,5-dimethyl-isoxazol-4-yl)-piperazin-1-yl-methanone. LR-MS: 210.2 [(M+H)+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07705007B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-827f2877858b4fdb975514df37f0b2cf
Quellennotizuspto-grants-2010_04