Bis(2-Methoxyethyl)amine → 3-[[Bis(2-methoxyethyl)amino]methyl]-2-(4-methoxyphenylmethyl)-2H-thieno[3,2-e]-1,2-thiazine 1,1-dioxide
反応式
O[CH2:2][C:3]1(CO)[CH2:8][C:7]2[CH:9]=[CH:10][S:11][C:6]=2[S:5](=[O:13])(=[O:12])[N:4]1[CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1.C(N(CC)CC)C.CS(OS(C)(=O)=O)(=O)=O.[CH3:41][O:42][CH2:43][CH2:44][NH:45][CH2:46][CH2:47][O:48][CH3:49]>C1COCC1>[CH3:41][O:42][CH2:43][CH2:44][N:45]([CH2:2][C:3]1[N:4]([CH2:14][C:15]2[CH:16]=[CH:17][C:18]([O:21][CH3:22])=[CH:19][CH:20]=2)[S:5](=[O:13])(=[O:12])[C:6]2[S:11][CH:10]=[CH:9][C:7]=2[CH:8]=1)[CH2:46][CH2:47][O:48][CH3:49]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of the product from Step C (1.60 g, 4.75 mmol) and triethylamine (1.44 g, 14.2 mmol) in anhydrous THF (100 mL) at ambient temperature was added methanesulfonic anhydride (1.24 g, 7.13 mmol). After 1 h, the reaction mixture was divided into two equal portions; to one of these portions was added bis(2-methoxyethyl)amine (6 mL). The mixture was stirred for 72 h, evaporated to dryness and the residue extracted with ethyl acetate (2×100 mL). The combined extracts were dried (MgSO4), filtered and evaporated to a residue which was purified by column chromatography (silica, 20-30% ethyl acetate/hexane) to give an oil (0.71 g) which solidified upon standing: mp 75°-77° C.
後処理
- customevaporated to dryness
- extractionthe residue extracted with ethyl acetate (2×100 mL)
- dry with materialThe combined extracts were dried (MgSO4)
- filtrationfiltered
- customevaporated to a residue which
- customwas purified by column chromatography (silica, 20-30% ethyl acetate/hexane)
出典と根拠
- ORDレコード
- ord-5c385ab44b184238ab3e5f53550ba0d5
- 出典データセット
- uspto-grants-1996_07
- 特許番号
- US05538966
反応ノート
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