Hydrochloric Acid → HCID 135456120, 화합물

HRID 1272435노트

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HRID 1272435 반응식
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]

참가 물질

5

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-d5491b45a78e490bb1a2b1fb5f29efac
출처 데이터셋
uspto-grants-2007_04
특허 번호
US07208524B2

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