Sodium Carbonate → 1-[1-[2-(6,7-Dichloro-1,4-benzodioxan-2-yl)-ethyl]-4-piperidyl]-2-imidazolidinone
反応式
S(O[CH2:12][CH2:13][CH:14]1[O:19][C:18]2[CH:20]=[C:21]([Cl:25])[C:22]([Cl:24])=[CH:23][C:17]=2[O:16][CH2:15]1)(C1C=CC(C)=CC=1)(=O)=O.[NH:26]1[CH2:31][CH2:30][CH:29]([N:32]2[CH2:36][CH2:35][NH:34][C:33]2=[O:37])[CH2:28][CH2:27]1.C(=O)([O-])[O-].[Na+].[Na+]>CC(C)CC(=O)C>[Cl:24][C:22]1[C:21]([Cl:25])=[CH:20][C:18]2[O:19][CH:14]([CH2:13][CH2:12][N:26]3[CH2:27][CH2:28][CH:29]([N:32]4[CH2:36][CH2:35][NH:34][C:33]4=[O:37])[CH2:30][CH2:31]3)[CH2:15][O:16][C:17]=2[CH:23]=1参加物
5
実験手順
The mixture of 4.0 g of 2-(2-tosyloxyethyl)-6,7-dichloro-1,4-benzodioxan, 1.69 g of 1-(4-piperidyl)-2-imidazolidinone, 10 g of ahydrous sodium carbonate and 100 ml of 4-methyl-2-pentanone is stirred and refluxed for 2 days. It is filtered, evaporated and the residue recrystallized from acetone, to yield the 1-[1-[2-(6,7-dichloro-1,4-benzodioxan-2-yl)-ethyl]-4-piperidyl]-2-imidazolidinone melting at 165°.
後処理
- temperaturerefluxed for 2 days
- filtrationIt is filtered
- customevaporated
- customthe residue recrystallized from acetone
出典と根拠
- ORDレコード
- ord-fe249e3b45b5408c9008579f5cb8c758
- 出典データセット
- uspto-grants-1982_05
- 特許番号
- US04329348
反応ノート
読み込み中…