Ethylamine → 2-Cyclopentyl-4-(((N-ethyl)amino)methyl)thiazole
反応式
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]1参加物
3
実験手順
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.
後処理
- customprovided
- customafter purification of the residue by silica gel chromatography
出典と根拠
- ORDレコード
- ord-33a5526393a74a289ed9e800ce2c5967
- 出典データセット
- uspto-grants-1999_03
- 特許番号
- US05886036
反応ノート
読み込み中…