Hydrochloric Acid → HCID 19834637, compound

HRID 2051060Notes

Reaction equation

HRID 2051060 reaction equation
C([O-])(=O)C.[NH4+].Cl.[CH3:7][NH:8][C:9]1[C:10]([O:19][CH3:20])=[C:11]([NH2:18])[C:12]([O:16][CH3:17])=[C:13]([Cl:15])[CH:14]=1.C1N2CCN(CC2)C1.Cl>[Pd].O.C(OCC)(=O)C.C(O)C.C(O)=O>[ClH:15].[CH3:7][NH:8][C:9]1[CH:14]=[CH:13][C:12]([O:16][CH3:17])=[C:11]([NH2:18])[C:10]=1[O:19][CH3:20]

Participants

10

Conditions

Temperature
70 °C

Procedure

The mixture consisting of 8.5 g of ammonium acetate, 7.5 g of 10% palladium on charcoal, 0.05 mole (15 g) of 5-methylamino-3-amino-2,4-dimethoxychlorobenzene hydrochloride in 14 ml of water containing 90 ml of ethanol and 15.2 g of triethylenediamine, was heated to 70° C. with stirring, and then 6.44 g of formic acid were added dropwise. Heating was maintained for 1 hour after completion of the addition. The catalyst was removed by filtration. The solids content obtained by evaporation of the filtrate under vacuum was dissolved in ethyl acetate. A 7N hydrochloric acid solution in absolute ethanol was added to the ethyl acetate which had been dried over sodium sulphate, in order to precipitate the expected product. The latter was recrystallized while hot from an aqueous-alcoholic solution of hydrochloric acid.

Workup

  1. temperatureHeating
  2. temperaturewas maintained for 1 hour
  3. additionafter completion of the addition
  4. customThe catalyst was removed by filtration
  5. customThe solids content obtained by evaporation of the filtrate under vacuum
  6. dry with materialhad been dried over sodium sulphate, in order
  7. customto precipitate the expected product
  8. customThe latter was recrystallized while hot from an aqueous-alcoholic solution of hydrochloric acid

Sources & evidence

ORD record
ord-406a0c5cb2b14f1e84e4d829157989ab
Source dataset
uspto-grants-1991_05
Patent number
US05015772

Reaction notes

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