Methanesulfonic Acid → 1,4-Bis[5-(3,4,5-triethoxyphenyl)-2-pyridyl]hexahydro-1,4-diazepine dimethanesulfonate
反応式
[O:1]([C:4]1[CH:5]=[C:6]([C:16]2[CH:17]=[CH:18][C:19]([N:22]3[CH2:28][CH2:27][CH2:26][N:25]([C:29]4[CH:34]=[CH:33][C:32]([C:35]5[CH:40]=[C:39]([O:41][CH2:42][CH3:43])[C:38]([O:44][CH2:45][CH3:46])=[C:37]([O:47][CH2:48][CH3:49])[CH:36]=5)=[CH:31][N:30]=4)[CH2:24][CH2:23]3)=[N:20][CH:21]=2)[CH:7]=[C:8]([O:13][CH2:14][CH3:15])[C:9]=1[O:10][CH2:11][CH3:12])[CH2:2][CH3:3].[CH3:50][S:51]([OH:54])(=[O:53])=[O:52]>CO>[CH3:50][S:51]([OH:54])(=[O:53])=[O:52].[CH3:50][S:51]([OH:54])(=[O:53])=[O:52].[CH2:48]([O:47][C:37]1[CH:36]=[C:35]([C:32]2[CH:33]=[CH:34][C:29]([N:25]3[CH2:26][CH2:27][CH2:28][N:22]([C:19]4[CH:18]=[CH:17][C:16]([C:6]5[CH:7]=[C:8]([O:13][CH2:14][CH3:15])[C:9]([O:10][CH2:11][CH3:12])=[C:4]([O:1][CH2:2][CH3:3])[CH:5]=5)=[CH:21][N:20]=4)[CH2:23][CH2:24]3)=[N:30][CH:31]=2)[CH:40]=[C:39]([O:41][CH2:42][CH3:43])[C:38]=1[O:44][CH2:45][CH3:46])[CH3:49]参加物
4
実験手順
To a solution of 1,4-bis[5-(3,4,5-triethoxylphenyl)-2-pyridyl]hexahydro-1,4-diazepine (77 mg, 0.115 mmol) in methanol (5.0 mL) was added a 1.0 M aqueous methanesulfonic acid (0.23 mL, 0.23 mmol), and the reaction mixture was concentrated under reduced pressure. Ethanol (5.0 mL) was added to the residue, and the resulting mixture was concentrated under reduced pressure. The residue was recrystallized from methanol-diethyl ether to yield the title compound as a pale yellow crystalline powder (melting point: 235.0-237.0° C.) (74.0 mg, yield: 94%).
後処理
- concentrationthe reaction mixture was concentrated under reduced pressure
- additionEthanol (5.0 mL) was added to the residue
- concentrationthe resulting mixture was concentrated under reduced pressure
- customThe residue was recrystallized from methanol-diethyl ether
出典と根拠
- ORDレコード
- ord-837cc1f0d66546d0a7a435edf2e40bf1
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06706703B2
反応ノート
読み込み中…