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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 405796Erstellt: 24. Oktober 2026

Bis-(1H-imidazol-2-YL)-methanone → Tert-butyl (3-(3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)oxetan-3-yl)carbamate

https://huagongshe.com/de/reaction/405796

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Edukt3-(Boc-amino)oxetane-3-carboxylic acidHCID 56592969—
EduktN-(5-(N'-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 86677441—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktTert-butyl (3-(3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)oxetan-3-yl)carbamateHCID 7128107565%

Reaktionsbedingungen

Temperatur125 °C

Reaktionsschritte

Carbonyl diimidazole (CDI) (162.2 mg, 1.0 mmol) was added to a stirred solution of 3-((tert-butoxycarbonyl)amino)oxetane-3-carboxylic acid (45) (217.1 mg, 1.0 mmol)) in NMP (1.0 mL). After 20 minutes, N-(5-(N′-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (9) (150.0 mg, 0.5 mmol) was added in one portion and the resulting solution was stirred for 1 hour before it was heated at 125° C. for 15 minutes in a microwave reactor. The reaction solution was subjected to standard aqueous work up to afford a residue which was purified by silica chromatography to yield tert-butyl (3-(3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)oxetan-3-yl)carbamate (46) (159 mg, 65% yield). MS m/z 491.2 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754071B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-941553a6c04141069044538e7f524bb2
Quellennotizuspto-grants-2014_06