Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH:12]([C:13]3[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][CH:14]=3)[NH:11][C:10]([C:20]3[C:21]([O:26][CH2:27][CH3:28])=[N:22][CH:23]=[CH:24][CH:25]=3)=[N:9]2)=[CH:4][CH:3]=1.C(N(CC)CC)C.[C:36](Cl)([Cl:38])=[O:37]>C(Cl)Cl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]2[CH:12]([C:13]3[CH:14]=[CH:15][C:16]([Cl:19])=[CH:17][CH:18]=3)[N:11]([C:36]([Cl:38])=[O:37])[C:10]([C:20]3[C:21]([O:26][CH2:27][CH3:28])=[N:22][CH:23]=[CH:24][CH:25]=3)=[N:9]2)=[CH:6][CH:7]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To a solution of 4,5-bis-(4-chloro-phenyl)-2-(2-ethoxy-pyridin-3-yl)-4,5-dihydro-1H-imidazole (475 mg, 1.152 mmol) and triethylamine (321 uL, 2.304 mmol) in methylene chloride (6 mL) cooled to 0° C. was added phosgene (895 uL, 1.728 mmol, 20% solution in toluene, Fluka). The reaction mixture was stirred at 0° C. for 30 min then concentrated to dryness. The residue was taken in ethyl acetate, and the solids were filtered off. The filtrate was concentrated to give crude 4,5-bis-(4-chloro-phenyl)-2-(2-ethoxy-pyridin-3-yl)-4,5-dihydro-imidazole-1-carbonyl chloride as yellow solids (450 mg).
Aufarbeitung
- concentrationthen concentrated to dryness
- filtrationthe solids were filtered off
- concentrationThe filtrate was concentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-4955c73f8fd54948993b495cd9fa144b
- Quelldatensatz
- uspto-grants-2010_04
- Patentnummer
- US07705007B2
Verknüpfte Notizen
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