Sodium Hydroxide → 2,2,7-Trimethyl-1,3-dioxolo-[4,5-g]-quinoxaline-6-carboxylic acid, 1,1-dimethylethyl ester

HRID 725246Notes

Reaction equation

HRID 725246 reaction equation
[NH2:1][C:2]1[C:12]([NH2:13])=[CH:11][C:5]2[O:6][C:7]([CH3:10])([CH3:9])[O:8][C:4]=2[CH:3]=1.C1(N)C(F)=C(F)C(F)=C(N)C=1F.Cl.Cl.[OH-].[Na+].[C:30]([O:34][C:35](=[O:41])[C:36](=O)[C:37](=O)[CH3:38])([CH3:33])([CH3:32])[CH3:31]>O.O1CCCC1>[CH3:9][C:7]1([CH3:10])[O:6][C:5]2=[CH:11][C:12]3[N:13]=[C:37]([CH3:38])[C:36]([C:35]([O:34][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:41])=[N:1][C:2]=3[CH:3]=[C:4]2[O:8]1

Participants

7

Procedure

[5,6-diamino-2,2-dimethyl-1,3-benzodioxole; dihydrochloride salt] (U.S. Pat. No. 4,904,775, Example 3D) (6.8 g, 0.02 mmol) was dissolved in a mixture of 25 ml water and 10 ml tetrahydrofuran and the pH of the solution was adjusted to 5.5 by the addition of 2N NaOH. After addition of the compound from Example 1 (3.8 g; 0.02 mol) the mixture was refluxed for 2 hours, concentrated in vacuo to remove the organic solvent tetrahydrofuran and then extracted with ethyl acetate. The combined organic phases were washed with brine, dried (Na2SO4) and then evaporated in vacuo to leave an oil which crystallized by the addition of petroleum ether. M.P. 104°-105° C.; yield 5.2 g (82%). C17H20N2O4 % C calc. 64.54%, found 64.40% % H calc. 6.37%, found 6.41% % N calc. 8.85%, found 8.86%

Workup

  1. temperaturewas refluxed for 2 hours
  2. concentrationconcentrated in vacuo
  3. customto remove the organic solvent tetrahydrofuran
  4. extractionextracted with ethyl acetate
  5. washThe combined organic phases were washed with brine
  6. dry with materialdried (Na2SO4)
  7. customevaporated in vacuo
  8. customto leave an oil which
  9. customcrystallized by the addition of petroleum ether

Sources & evidence

ORD record
ord-699b74c1d37f48d3956f8cfc88094db9
Source dataset
uspto-grants-1998_01
Patent number
US05705645

Reaction notes

Loading…