HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1672470Erstellt: 26. Oktober 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 178521594, Verbindung
https://huagongshe.com/reaction/1672470
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | 8-Bromo-2-chloroquinazoline | HCID 45790061 | — |
| Edukt | HCID 178511715 | HCID 178511715 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | HCID 178521594 | HCID 178521594 | 35% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07998978B2 |
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| Quelldatensatz | uspto-grants-2011_08 |
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| ORD ID | ord-f8c505d937f4476b9115cfed19668f52 |
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| Quellennotiz | uspto-grants-2011_08 |
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