反応式
[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([CH2:10][NH:11][C:12]2[S:13][C:14]3[CH:20]=[CH:19][CH:18]=[CH:17][C:15]=3[N:16]=2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2].[H-].[Na+].[CH3:23]N(C)C=O.IC>O>[C:1]([N:4]1[CH2:5][CH2:6][CH:7]([CH2:10][N:11]([C:12]2[S:13][C:14]3[CH:20]=[CH:19][CH:18]=[CH:17][C:15]=3[N:16]=2)[CH3:23])[CH2:8][CH2:9]1)(=[O:3])[CH3:2]参加物
実験手順
A mixture of 8.7 parts of 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine, 1.44 parts of a sodium hydride dispersion 60% and 270 parts of N,N-dimethylformamide was stirred for 1 hour at room temperature. 5.48 Parts of iodomethane were added dropwise slowly. Upon completion, stirring was continued overnight at room temperature. The reaction mixture was poured into water. The product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated in vacuo. The residue was purified by column chromatography (HPLC) over silica gel using a mixture of dichloromethane and methanol (98.75:1.25 by volume) as eluent. The second fraction was collected and the eluent was evaporated, yielding 7.6 parts (84%) of 1-acetyl-N-(2-benzothiazolyl)-N-methyl-4-piperidinemethanamine as a residue (intermediate 52).
後処理
- stirringUpon completion, stirring
- waitwas continued overnight at room temperature
- extractionThe product was extracted with 4-methyl-2-pentanone
- customThe extract was dried
- filtrationfiltered
- customevaporated in vacuo
- customThe residue was purified by column chromatography (HPLC) over silica gel using
- additiona mixture of dichloromethane and methanol (98.75:1.25 by volume) as eluent
- customThe second fraction was collected
- customthe eluent was evaporated
出典と根拠
- ORDレコード
- ord-7cd75d0429bf4d87af5fa3b11ba8793d
- 出典データセット
- uspto-grants-1989_05
- 特許番号
- US04826848
関連ノート
読み込み中…