Sodium Hydroxide → HCID 69894550, compound

HRID 353204Notes

Reaction equation

HRID 353204 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10](=[O:33])[CH2:11][N:12]([CH2:19][C:20]1[CH:32]=[CH:31][C:23]([O:24][C:25]([CH3:30])([CH3:29])[C:26]([OH:28])=[O:27])=[CH:22][CH:21]=1)[CH2:13][C:14]1[O:15][CH:16]=[CH:17][CH:18]=1.[OH-].[Na+:35]>C(O)C>[Na+:35].[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10](=[O:33])[CH2:11][N:12]([CH2:19][C:20]1[CH:21]=[CH:22][C:23]([O:24][C:25]([CH3:30])([CH3:29])[C:26]([O-:28])=[O:27])=[CH:31][CH:32]=1)[CH2:13][C:14]1[O:15][CH:16]=[CH:17][CH:18]=1

Participants

4

Procedure

0.015 g (0.03 mmol) of the compound from Example 3-4 is dissolved in 0.5 ml of ethanol and treated with 0.3 ml of 1N aqueous sodium hydroxide solution. The reaction mixture is stirred for another 5 min and then concentrated using a rotary evaporator. The residue is taken up in a little toluene and the solvent is removed under reduced pressure. The product is then dried under reduced pressure for 20 hours. This gives 0.015 g (95.5% of theory) of the title compound.

Workup

  1. concentrationconcentrated
  2. customa rotary evaporator
  3. customthe solvent is removed under reduced pressure
  4. customThe product is then dried under reduced pressure for 20 hours

Sources & evidence

ORD record
ord-cc86c84946ec48dfab81ceeb57e9abbd
Source dataset
uspto-grants-2004_06
Patent number
US06750236B2

Reaction notes

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