Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76334Erstellt: 24. Oktober 2026

Imidazole → HCID 178481629, Verbindung

https://huagongshe.com/de/reaction/76334

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktChlorotrimethylsilaneHCID 6397—
EduktBenzylamineHCID 7504—
EduktTriethylamineHCID 8471—
Edukt1-Methylimidazolidine-2,4,5-trioneHCID 123196—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
ProduktHCID 178481629HCID 17848162962%

Reaktionsschritte

To a solution of 1-methyl-imidazolidine-2,4,5-trione (Example 1.3, Part A) (800 mg, 6.25 mmol), imidazole (467 mg, 6.87 mmol), N,N-dimethylaminopyridine (cat.) and triethylamine (1.82 mL, 13.1 mmol) in chloroform (13 mL) was added chlorotrimethylsilane (1.67 mL, 13.1 mmol) dropwise at room temperature under a nitrogen atmosphere, and the reaction mixture was stirred for 2 h. Benzylamine (0.75 mL, 6.87 mmol) was added and the reaction mixture was stirred for a further 22.5 h. The reaction mixture was diluted with chloroform and water and the chloroform extracts were dried and evaporated. The crude product was purified by column chromatography (PS with gradient elution to DCM:EtOAc 3:1) to give the product as a colourless solid (838 mg, 62%), mp 152-154° C. δH (300 MHz, CD3CN) 7.95 (v br s, 1H, NH), 7.41-7.27 (m, 5H, PhH), 4.64 (s, 2H, CH2), 2.95 (s, 3H, CH3). Mass spectrum (ESI) m/z 218 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835629B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-acce0bf81faf4463902c8f37549108b5
Quellennotizuspto-grants-2014_09