Ethylamine → 2-Cyclopentyl-4-(((N-ethyl)amino)methyl)thiazole
Reaction equation
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]1Participants
3
Procedure
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.
Workup
- customprovided
- customafter purification of the residue by silica gel chromatography
Sources & evidence
- ORD record
- ord-f764af7e51b84234a3a5484d3300f58d
- Source dataset
- uspto-grants-1997_10
- Patent number
- US05679797
Reaction notes
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