Thionyl Chloride → HCID 59561810, Verbindung
Reaktionsgleichung
[C:1]([O:5][C:6](=[O:25])[NH:7][CH2:8][C:9]1[CH:24]=[CH:23][C:12]2[N:13]([CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21])[C:14]([CH2:16]O)=[N:15][C:11]=2[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].S(Cl)([Cl:28])=O>C(Cl)Cl>[C:1]([O:5][C:6](=[O:25])[NH:7][CH2:8][C:9]1[CH:24]=[CH:23][C:12]2[N:13]([CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21])[C:14]([CH2:16][Cl:28])=[N:15][C:11]=2[CH:10]=1)([CH3:4])([CH3:3])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To a cooled (0° C.) solution of [2-hydroxymethyl-1-(3-methyl-butyl)-1H-benzoimidazol-5-ylmethyl]-carbamic acid tert-butyl ester (146 mg, 0.42 mmol) in DCM (5 mL) was added thionyl chloride (46 μL, 0.63 mmol). The solution was stirred at 0° C. for 15 min. and concentrated in vacuo to give [2-chloromethyl-1-(3-methyl-butyl)-1H-benzoimidazol-5-ylmethyl]-carbamic acid tert-butyl ester; HCl salt (176 mg, 100%) as a white solid, which was used without further purification.