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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1672470Erstellt: 25. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 178521594, Verbindung

https://huagongshe.com/reaction/1672470

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt8-Bromo-2-chloroquinazolineHCID 45790061—
EduktHCID 178511715HCID 178511715—
LösungsmittelAcetonitrileHCID 6342—
ProduktHCID 178521594HCID 17852159435%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

To a solution of 8-bromo-2-chloroquinazoline (7.3 g, 30 mmol) in acetonitrile (150 mL) was added trans-4-aminocyclohexanol (6.9 g, 60 mmol) to form a suspension. DBU (9.1 g, 60 mmol) was added. The reaction mixture was stirred at 45° C. overnight. A light yellow suspension was formed. The solvent was removed under reduced pressure, and the residue was taken into DCM (100 mL) and washed with water (100 mL). The organic layer was dried over Na2SO4 and purified by chromatography (eluting with DCM) to give the title compound as a light yellow solid (3.36 g, 35%). 1HNMR (DMSO-d6, 400 MHz): δ 9.10 (s, 1H), 8.02 (dd, J=1.2, 7.6 Hz, 1H), 7.81 (dd, J=1.2, 7.6 Hz, 1H), 7.62-7.60 (m, 1H), 7.12 (dd, J=7.6, 7.6 Hz, 1H), 4.62-4.60 (m, 1H), 3.85-3.82 (m, 1H), 2.05-2.02 (m, 2H), 1.89-1.86 (m, 2H), 1.36-1.26 (m, 4H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07998978B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-f8c505d937f4476b9115cfed19668f52
Quellennotizuspto-grants-2011_08