Methanesulfonic Acid → 1,4-Bis[5-(3,5-dimethylphenyl)-2-pyridyl]hexahydro-1,4-diazepine dimethanesulfonate

HRID 460381ノート

反応式

HRID 460381 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:10]=[CH:11][C:12]([N:15]3[CH2:21][CH2:20][CH2:19][N:18]([C:22]4[CH:27]=[CH:26][C:25]([C:28]5[CH:33]=[C:32]([CH3:34])[CH:31]=[C:30]([CH3:35])[CH:29]=5)=[CH:24][N:23]=4)[CH2:17][CH2:16]3)=[N:13][CH:14]=2)[CH:5]=[C:6]([CH3:8])[CH:7]=1.[CH3:36][S:37]([OH:40])(=[O:39])=[O:38]>CO>[CH3:36][S:37]([OH:40])(=[O:39])=[O:38].[CH3:36][S:37]([OH:40])(=[O:39])=[O:38].[CH3:8][C:6]1[CH:5]=[C:4]([C:9]2[CH:10]=[CH:11][C:12]([N:15]3[CH2:21][CH2:20][CH2:19][N:18]([C:22]4[CH:27]=[CH:26][C:25]([C:28]5[CH:33]=[C:32]([CH3:34])[CH:31]=[C:30]([CH3:35])[CH:29]=5)=[CH:24][N:23]=4)[CH2:17][CH2:16]3)=[N:13][CH:14]=2)[CH:3]=[C:2]([CH3:1])[CH:7]=1

参加物

4

実験手順

To a solution of 1,4-bis[5-(3,5-dimethylphenyl)-2-pyridyl]hexahydro-1,4-diazepine (83.0 mg, 0.170 mmol) in methanol (5.0 mL) was added a 1.0 M aqueous methanesulfonic acid (0.37 mL, 0.37 mmol), and the 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 ethanol-diethyl ether-hexane to yield the title compound as colorless needles [melting point: 188.0° C. (decomposed)](101.0 mg, yield: 86%).

後処理

  1. concentrationthe mixture was concentrated under reduced pressure
  2. additionEthanol (5.0 mL) was added to the residue
  3. concentrationthe resulting mixture was concentrated under reduced pressure
  4. customThe residue was recrystallized from ethanol-diethyl ether-hexane

出典と根拠

ORDレコード
ord-7851f1f7ba1c427daf14866955ea3277
出典データセット
uspto-grants-2007_03
特許番号
US07196101B2

反応ノート

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