Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 331077Erstellt: 24. Oktober 2026

Isocyanate → HCID 59334017, Verbindung

https://huagongshe.com/de/reaction/331077

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsocyanateHCID 105034—
EduktTetrahydro-4H-pyran-4-oneHCID 121599—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt(2S,5R)-1-Benzyl-2,5-dimethylpiperazineHCID 23402345—
LösungsmittelEthanolHCID 702—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 59334017HCID 5933401784%

Reaktionsschritte

To a mixture of (2S,5R)-1-benzyl-2,5-dimethylpiperazine (11.0 g, 53.8 mmol) and of tetrahydro-4H-pyran-4-one (5.39 g, 53.8 mmol) at 0° C. was added Ti(IV) isopropoxide (19.2 mL, 67.3 mmol). The resulting mixture was stirred at rt overnight and an orange suspension was obtained. To the suspension was added EtOH (25 mL) and NaCNBH3 (4.27 g, 64.6 mmol, 1.20 eq). The resulting mixture was stirred at rt for 24 h. The reaction mixture was then quenched with water (5.0 mL) and a yellow solid was generated. The suspension was diluted with EtOAc (400 mL) and filtered. The filtrate was concentrated under reduced pressure. The residue was again diluted with EtOAc (500 mL), dried over Na2SO4, and filtered. The filtrate was collected and concentrated under reduced pressure to afford a yellow oil. The oil was diluted in THF (400 mL) and PS-isocyanate was added to remove secondary amine. The suspension was filtered and the filtrate concentrated. The residue was purified by column chromatography using 50:5:1 CHCl3/MeOH/Et3N to afford the desired compound as yellow oil (13.0 g, 84%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08877761B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-891eeedd9aca48aa80cc2734d6062d6b
Quellennotizuspto-grants-2014_11