Ethylamine → 2-Cyclopentyl-4-(((N-ethyl)amino)methyl)thiazole
Reaktionsgleichung
Cl.Cl[CH2:3][C:4]1[N:5]=[C:6]([CH:9]2[CH2:13][CH2:12][CH2:11][CH2:10]2)[S:7][CH:8]=1.[CH2:14]([NH2:16])[CH3:15]>>[CH:9]1([C:6]2[S:7][CH:8]=[C:4]([CH2:3][NH:16][CH2:14][CH3:15])[N:5]=2)[CH2:13][CH2:12][CH2:11][CH2:10]1Komponenten
3
Versuchsvorschrift
Using the procedure of Example 1Q, but replacing 4-(chloromethyl)-2-isopropylthiazole hydrochloride with 4-(chloromethyl)-2-cyclopentylthiazole hydrochloride and replacing 40% aqueous methylamine with 70% aqueous ethylamine provided, after purification of the residue by silica gel chromatography using 5% methanol in chloroform, 1.08 g (50%) of the desired compound.
Aufarbeitung
- customprovided
- customafter purification of the residue by silica gel chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-0a6c4c536bd649799e5f5e3370fffe9c
- Quelldatensatz
- uspto-grants-1996_12
- Patentnummer
- US05583232
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