Sodium Hydroxide → HCID 67975037, compound

HRID 1507385Notes

Reaction equation

HRID 1507385 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[C:8]([C:13]1[CH:22]=[CH:21][C:16]([C:17]([O:19]C)=[O:18])=[CH:15][CH:14]=1)[CH:7]=[N:6]2.[OH-].[Na+]>CO>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[C:8]([C:13]1[CH:22]=[CH:21][C:16]([C:17]([OH:19])=[O:18])=[CH:15][CH:14]=1)[CH:7]=[N:6]2

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 67974888HCID 67974888, compound

Product 1

HCID 67975037HCID 67975037, compoundYield 104.9%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
30 °C

Procedure

A mixture of methyl 4-(6-methoxyquinoxalin-2-yl)benzoate (80 mg, 0.272 mmol) and aqueous NaOH (5 mL, 2M) in MeOH (5 mL) was stirred at 30° C. overnight. The resulting mixture was concentrated in vacuo. The residue was acidified with aqueous HCl (2M) until pH=3 and concentrated. The solid was dissolved in MeOH (30 mL) and filtered. The filtrate was concentrated in vacuo to give crude product (80 mg), which was used for next step directly without further purification.

Workup

  1. concentrationThe resulting mixture was concentrated in vacuo
  2. concentrationconcentrated
  3. dissolutionThe solid was dissolved in MeOH (30 mL)
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated in vacuo

Sources & evidence

ORD record
ord-17ff09a1e0b24a26a3634eb7061f505a
Source dataset
uspto-grants-2015_12
Patent number
US09221810B2

Reaction notes

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