Sodium Hydroxide → Sodium [4-[2-(5-cyano-2-hydroxybenzenesulfonylamino)ethyl]-2'-methanesulfonylbiphenyl-3-yloxy]acetate

HRID 1272438Notes

Reaction equation

HRID 1272438 reaction equation
[C:1]([C:3]1[CH:4]=[CH:5][C:6]([OH:36])=[C:7]([S:9]([NH:12][CH2:13][CH2:14][C:15]2[CH:20]=[CH:19][C:18]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=3[S:27]([CH3:30])(=[O:29])=[O:28])=[CH:17][C:16]=2[O:31][CH2:32][C:33]([OH:35])=[O:34])(=[O:11])=[O:10])[CH:8]=1)#[N:2].[OH-].[Na+:38]>C(O)C>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([OH:36])=[C:7]([S:9]([NH:12][CH2:13][CH2:14][C:15]2[CH:20]=[CH:19][C:18]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=3[S:27]([CH3:30])(=[O:29])=[O:28])=[CH:17][C:16]=2[O:31][CH2:32][C:33]([O-:35])=[O:34])(=[O:10])=[O:11])[CH:8]=1)#[N:2].[Na+:38]

Participants

4

Procedure

To a stirred solution of 146 g of [4-[2-(5-cyano-2-hydroxybenzenesulfonylamino)ethyl]-2′-methanesulfonyl-biphenyl-3-yloxy]acetic acid in 580 mL of ethanol was added 137 mL of 2mol/L sodium hydroxide solution under ice-cooling, and the solvent was removed under reduced pressure. The residue was suspended with 1.16 L of ethanol, and the mixture was stirred under reflux for an hour, then at room temperature overnight. The obtained white solid was collected by filtration to give 129 g of sodium[4-[2-(5-cyano-2-hydroxybenzenesulfonyl-amino)ethyl]-2′-methanesulfonylbiphenyl-3-yloxy]acetate.

Workup

  1. temperaturecooling
  2. customthe solvent was removed under reduced pressure
  3. temperatureunder reflux for an hour
  4. customat room temperature
  5. customovernight
  6. filtrationThe obtained white solid was collected by filtration

Sources & evidence

ORD record
ord-4c56853a94044c8d84fd0f80231d8f15
Source dataset
uspto-grants-2007_04
Patent number
US07208524B2

Reaction notes

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