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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9110Erstellt: 24. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-(7-Hydroxy-2-benzothiazolyl)-3-ethyl-urea

https://huagongshe.com/de/reaction/9110

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt1-(6,6-Dibromo-7-oxo-4,5,6,7-tetrahydro-2-benzothiazolyl)-3-ethyl-ureaHCID 21985529—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(7-Hydroxy-2-benzothiazolyl)-3-ethyl-ureaHCID 2198552332,2%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

To a suspension of 1-(6-bromo-7-oxo-4,5,6,7-tetrahydro-2-benzothiazolyl)-3-ethyl-urea 5 (0.100 g, 0.314 mmol) in THF (1.0 mL) was added DBU (0.141 mL, 0.94 mmol, 3 eq) dropwise at about 20° C. A dark green suspension was obtained while heat was generated upon addition of DBU. It was stirred at about 20° C. for about 18 hours. The reaction mixture was concentrated and dissolved in DMF (2 mL). LC/MS purification gave 0.024 g (32%) of the desired compound 8. 1H NMR (DMSO) δ 10.54 (br s, 1H, NH), 7.17–7.07 (m, 2H, ArH), 6.63 (d, 1H, J=6.9 Hz, ArH), 6.70 (br s, 1H, NH), 3.18 (m, 2H, CH2), 1.09 (t, 3H, J=7.2 Hz, CH3). LC/MS 238 (MH+); RP-HPLC RT 2.26 minutes.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091227B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-f28c76dea7f44a58b87eb28465351440
Quellennotizuspto-grants-2006_08