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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 277777Erstellt: 24. Oktober 2026

Tetrahydrofuran → 1-(1-(4-Cyanobenzyl)imidazole-5-ylmethyl)-4-(tert-butyloxycarbonyl)-(trans)2,5-dimethylpiperazine

https://huagongshe.com/de/reaction/277777

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt4-[(5-Formylimidazol-1-yl)methyl]benzonitrileHCID 10632289—
Edukt(2R,5S)-2,5-Dimethyl-piperazine-1-carboxylic acid tert-butyl esterHCID 24903576—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelEthanolHCID 702—
LösungsmittelMethanol--water (1/1)HCID 22242641—
Produkt1-(1-(4-Cyanobenzyl)imidazole-5-ylmethyl)-4-(tert-butyloxycarbonyl)-(trans)2,5-dimethylpiperazineHCID 70153172—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a round bottom flask were added 1-(4-cyanobenzyl)-5-formylimidazole (250.0 mg, 1.2 mmole) along with titanium(IV)isopropoxide (1.0 ml, 3.65 mmol), (trans) 2,5-Dimethyl-4-tertbutyloxycarbonylpiprizine (253.7 mg, 1.2 mmol) (prepared as described in Step 1), and tetrahydrofuran (0.4 ml). The reaction was heated at 60° C. for 1.25 hour. The reaction was cooled and sodiumcyanoborohydride (95.0 mg, 1.5 mmol) was added along with ethanol (0.5 ml) and the reaction was stirred at RT for 18 hours. The reaction was diluted with methanol/water (3 ml/1 ml) and the mixture filtered through celite. The filtrate was then concentrated to an oil, dissolved into methanol and put through a High Pressure Liquid Chromatography column. The desired fractions were collected, concentrated, and lyophilized to give the ditrifluoroacetic acid salt of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06358956B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-746d9af315ab4fb7a69c9a5a5da08560
Quellennotizuspto-grants-2002_03