Sodium Hydroxide → HCID 178424829, compound

HRID 439798Notes

Reaction equation

HRID 439798 reaction equation
[NH2:1][C:2]1[N:3](C(=O)N)[N:4]=[CH:5][C:6]=1[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([CH3:20])[CH:15]=2)=[CH:9][CH:8]=1.[OH-].[Na+]>CO>[NH2:1][C:2]1[C:6]([C:7]2[CH:8]=[CH:9][C:10]([CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[C:16]([CH3:20])[CH:15]=3)=[CH:11][CH:12]=2)=[CH:5][NH:4][N:3]=1

Participants

4

Procedure

To a solution of 3-amino-2-carbamoyl-4-[4-(3-methylphenylmethyl) phenyl]pyrazole (2.0 g) in methanol (20 ml) was added 5N sodium hydroxide solution (10 ml), and the mixture was refluxed for 4 hours. Methanol was distilled away under reduced pressure. To the residue was added water (100 ml), and the mixture was neutralized (pH 7 to 8) with conc. hydrochloric acid, and extracted with chloroform. The extadt was washed with water and saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent was distilled away under reduced pressure. The residue was separated and purified by using a silica-gel column chromatography (ethyl acetate:n-hexane=1:1 followed by chloroform:methanol=10:1) to give a mixture containing the title compound. This mixture was used in the subsequent reaction without isolation.

Workup

  1. temperaturethe mixture was refluxed for 4 hours
  2. distillationMethanol was distilled away under reduced pressure
  3. additionTo the residue was added water (100 ml)
  4. extractionextracted with chloroform
  5. washThe extadt was washed with water and saturated aqueous sodium chloride solution
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationthe solvent was distilled away under reduced pressure
  8. customThe residue was separated
  9. custompurified
  10. customto give a mixture

Sources & evidence

ORD record
ord-838727dd27b443c6bfa7b5dfdf9d6137
Source dataset
uspto-grants-1996_05
Patent number
US05516777

Reaction notes

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