Sodium Hydroxide → HCID 69699735, compound

HRID 1061056Notes

Reaction equation

HRID 1061056 reaction equation
Cl.[Cl:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([S:13]([N:16]1[CH2:21][CH2:20][N:19]([C:22](=[O:35])[C:23]3[CH:28]=[CH:27][C:26]([C:29]4[CH:34]=[CH:33][N:32]=[CH:31][CH:30]=4)=[CH:25][CH:24]=3)[CH:18]([C:36]([O:38]CC)=[O:37])[CH2:17]1)(=[O:15])=[O:14])[CH:7]=[CH:6]2.[OH-].[Na+]>C(O)C.O1CCCC1.O>[ClH:2].[Cl:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([S:13]([N:16]1[CH2:21][CH2:20][N:19]([C:22](=[O:35])[C:23]3[CH:28]=[CH:27][C:26]([C:29]4[CH:34]=[CH:33][N:32]=[CH:31][CH:30]=4)=[CH:25][CH:24]=3)[CH:18]([C:36]([OH:38])=[O:37])[CH2:17]1)(=[O:15])=[O:14])[CH:7]=[CH:6]2

Participants

6

Procedure

In a mixed solvent of ethanol (1 ml), tetrahydrofuran (1 ml) and water (1 ml), 4-[(6-chloronaphthalen-2-yl)sulfonyl]-2-ethoxycarbonyl-1-[4-(pyridin-4-yl)benzoyl]piperazine hydrochloride (152 mg) obtained in Example 2 was dissolved under ice cooling, followed by the dropwise addition of a 1N aqueous solution of sodium hydroxide. The reaction mixture was stirred at room temperature for 90 minutes. After concentration under reduced pressure, 1N hydrochloric acid was added to the reaction mixture to make it weakly acidic. The colorless solid so precipitated was collected by filtration, followed by drying, whereby the title compound (62 mg, 42%) was obtained as a colorless solid.

Workup

  1. concentrationAfter concentration under reduced pressure, 1N hydrochloric acid
  2. additionwas added to the reaction mixture
  3. customThe colorless solid so precipitated
  4. filtrationwas collected by filtration
  5. customby drying

Sources & evidence

ORD record
ord-6d333c335c184cc89cd52527efed4b0d
Source dataset
uspto-grants-2003_02
Patent number
US06525042B1

Reaction notes

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