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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 967824Erstellt: 25. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 10239024, Verbindung

https://huagongshe.com/reaction/967824

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt5-Methyl-2-pyridinesulfonamideHCID 3614199—
Eduktphenyl 2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethylcarbamateHCID 22291379—
LösungsmittelAcetonitrileHCID 6342—
ProduktHCID 10239024HCID 1023902460%

Reaktionsschritte

A mixture of phenyl 2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethylcarbamate (203 mg, 0.50 mmol), 5-methylpyridine-2-sulfonamide (86 mg, 0.50 mmol) and DBU (82 μL, 0.55 mmol) in acetonitrile (5 mL) was stirred for overnight at ambient temperature. Then, the volatile components were removed by evaporation and the residue was dissolved in dichloromethane. The organic phase was washed with water, dried (MgSO4) and concentrated. The residue was purified by TLC with dichloromethane/methanol (10:1) to afford 145 mg (60%) of the title compound as white solids: MS (ESI) m/z 490 [M+H]+, 488 [M−H]−, 1H-NMR (DMSO-d6) δ 1.18 (3H, t, J=7.5 Hz), 2.37 (3H, s), 2.72-2.90 (4H, m), 3.23 (2H, q, J=6.0 Hz), 6.69 (1H, br), 7.40-7.59 (6H, m), 7.85-7.93 (4H, m), 8.24 (1H, s), 8.55 (1H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06956050B2
Quelldatensatzuspto-grants-2005_10
ORD IDord-11124db4cd74422f8dfa75777f7927a4
Quellennotizuspto-grants-2005_10