2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester → HCID 19089095, compound

HRID 1463983Notes

Reaction equation

HRID 1463983 reaction equation
C(OC(=O)C(=COCC)C#N)C.C(OC(OCC)C(NN)C)C.[CH3:24][CH:25]([N:33]1[C:37]([NH2:38])=[C:36]([C:39]([O:41]CC)=[O:40])[CH:35]=[N:34]1)[CH:26]([O:30][CH2:31][CH3:32])[O:27][CH2:28][CH3:29]>C(O)C.[OH-].[Na+]>[CH3:24][CH:25]([N:33]1[C:37]([NH2:38])=[C:36]([C:39]([OH:41])=[O:40])[CH:35]=[N:34]1)[CH:26]([O:30][CH2:31][CH3:32])[O:27][CH2:28][CH3:29]

Participants

6

Procedure

To a solution of 2-(ethoxymethylene)-2-cyanoacetic acid ethyl ester (56.3 g) in ethanol (200 ml) was added dropwise 2-hydrazinopropionaldehyde diethyl acetal (54 g) in ethanol (80 ml) at room temperature. The mixture was refluxed for 4 hours. The reaction mixture was cooled at room temperature and the solvent was distilled off in vacuo to give the crude. 1-(1-methyl-2,2-diethoxyethyl)-4-ethoxycarbonyl-5-aminopyrazole (100 g). The crude product (100 g) was dissolved in aqueous 4N-sodium hydroxide (170 ml) and the mixture was refluxed for 1 hour. The reaction mixture was cooled at room temperature and washed with ethyl acetate (100 ml×2). The aqueous solution was adjusted to pH 3.5 with 6N-hydrochloric acid and stirred for 1 hour. The precipitate was collected by filtration, washed with water and dried over phosphorus pentoxide to give 1-(1-methyl-2,2-diethoxyethyl)-4-carboxy-5-aminopyrazole (9.93 g).

Workup

  1. temperatureThe mixture was refluxed for 4 hours
  2. distillationthe solvent was distilled off in vacuo
  3. customto give the crude
  4. temperaturethe mixture was refluxed for 1 hour
  5. temperatureThe reaction mixture was cooled at room temperature
  6. washwashed with ethyl acetate (100 ml×2)
  7. filtrationThe precipitate was collected by filtration
  8. washwashed with water
  9. dry with materialdried over phosphorus pentoxide

Sources & evidence

ORD record
ord-90d6664a06b24ebaa6e8b9b1b6bb2170
Source dataset
uspto-grants-1994_04
Patent number
US05302712

Reaction notes

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