Methanol → HCID 22918419, compound

HRID 2396063Notes

Reaction equation

HRID 2396063 reaction equation
C[O:2][C:3](=[O:32])[C:4]1[C:5](=[CH:10][C:11]([NH:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[C:12]([NH:14][C:15]2[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:16]=2[O:23][CH3:24])[CH:13]=1)[C:6]([O:8]C)=[O:7].CO.O.[OH-].[Li+].O=C1O[C@H]([C@H](CO)O)C([O-])=C1O.[Na+]>O>[NH:25]([C:11]1[CH:10]=[C:5]([C:6]([OH:8])=[O:7])[C:4](=[CH:13][C:12]=1[NH:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:16]=1[O:23][CH3:24])[C:3]([OH:32])=[O:2])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1

Participants

6

Procedure

A steady stream of argon is passed through a suspension of 479 mg (1.09 mmol) of 4-anilino-5-(2,4-dimethoxy-anilino)phthalic acid dimethylester in3.6 ml of methanol, and a solution of 205 mg (4.905 mmol, 4.5 eq) of lithium hydroxide monohydrate and 10 mg sodium ascorbate in 1.7 ml of water is added. The reaction mixture is heated to reflux for 4 hours, cooled to RT, and the methanol is removed by evaporation. The resulting mixture is poured onto 20 ml of 4N hydrochloric acid, the red suspension is filtered and the crystals are washed with washed with isopropanol/hexane 1:5 to yield the title compound in the form of red crystals, TLC (dichloromethane/methanol 7:3) Rf =0.33.

Workup

  1. temperatureThe reaction mixture is heated
  2. temperatureto reflux for 4 hours
  3. customthe methanol is removed by evaporation
  4. additionThe resulting mixture is poured onto 20 ml of 4N hydrochloric acid
  5. filtrationthe red suspension is filtered
  6. washthe crystals are washed
  7. washwith washed with isopropanol/hexane 1:5

Sources & evidence

ORD record
ord-15f5c8eb4a6b4bddabaeb644ad905e3d
Source dataset
uspto-grants-1996_02
Patent number
US05491144

Reaction notes

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