Hydrochloric Acid → HCID 135456120, Verbindung

HRID 1272435Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1272435
C([O:3][C:4](=[O:39])[CH2:5][O:6][C:7]1[CH:8]=[C:9]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=2[S:35]([CH3:38])(=[O:37])=[O:36])[CH:10]=[CH:11][C:12]=1[CH2:13][CH2:14][NH:15][S:16]([C:19]1[CH:24]=[C:23]([C:25](=[NH:27])[NH2:26])[CH:22]=[CH:21][C:20]=1[OH:28])(=[O:18])=[O:17])C.[OH-].[Na+].[ClH:42]>C(#N)C>[ClH:42].[C:25]([C:23]1[CH:22]=[CH:21][C:20]([OH:28])=[C:19]([S:16]([NH:15][CH2:14][CH2:13][C:12]2[CH:11]=[CH:10][C:9]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=3[S:35]([CH3:38])(=[O:37])=[O:36])=[CH:8][C:7]=2[O:6][CH2:5][C:4]([OH:39])=[O:3])(=[O:17])=[O:18])[CH:24]=1)(=[NH:26])[NH2:27]

Komponenten

5

Versuchsvorschrift

To a solution of 290 mg of ethyl[4-[2-(5-carbamimidoyl-2-hydroxybenzenesulfonylamino)ethyl]-2′-methanesulfonoylbiphenyl-3-yloxy]acetate in 1.0 mL of acetonitrile was added 0.756 mL of 2 mol/L sodium hydroxide solution, and the mixture was stirred at room temperature for 30 minutes. To the reaction mixture was added 1.26 mL of 2 mol/L hydrochloric acid, and the mixture was concentrated under reduced pressure. To the residue was added water, and the mixture was purified by column chromatography on trimethylaminopropylated silica gel (eluent: 10% lmol/L hydrochloric acid-acetonitrile). The eluent was concentrated under reduced pressure to give 260 mg of [4-[2-(5-carbamimidoyl-2-hydroxybenzenesulfonylamino)-ethyl]-2′-methanesulfonoylbiphenyl-3-yloxy]acetic acid hydrochloride as a white solid.

Aufarbeitung

  1. concentrationthe mixture was concentrated under reduced pressure
  2. additionTo the residue was added water
  3. customthe mixture was purified by column chromatography on trimethylaminopropylated silica gel (eluent
  4. concentrationThe eluent was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-d5491b45a78e490bb1a2b1fb5f29efac
Quelldatensatz
uspto-grants-2007_04
Patentnummer
US07208524B2

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