Potassium Hydroxide → HCID 13882135, compound

HRID 867385Notes

Reaction equation

HRID 867385 reaction equation
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[N:9]1[C:13]([C:14]#[N:15])=[C:12]([C:16]([O:18]CC)=[O:17])[CH:11]=[N:10]1.[OH-:21].[K+]>C(O)C>[C:16]([C:12]1[CH:11]=[N:10][N:9]([C:3]2[CH:4]=[CH:5][CH:6]=[C:7]([Cl:8])[C:2]=2[Cl:1])[C:13]=1[C:14]([NH2:15])=[O:21])([OH:18])=[O:17]

Participants

4

Procedure

A 15 g. portion of ethyl 1-(2,3-dichlorophenyl)-5-cyano-4-pyrazolecarboxylate was stirred under reflux overnight in 200 ml. of ethanol with 6 g. of potassium hydroxide. The reaction mixture was chromatographed over silica gel, and the product-containing fractions were combined and evaporated to dryness. The residues were recrystallized from ethanol-water to obtain 1.31 g. of the desired product, m.p. 228°-230°, which was identified by elemental analysis.

Workup

  1. temperatureunder reflux overnight in 200 ml
  2. customThe reaction mixture was chromatographed over silica gel
  3. customevaporated to dryness
  4. customThe residues were recrystallized from ethanol-water
  5. customto obtain 1.31 g

Sources & evidence

ORD record
ord-c6dec9ada87f4a4aad1b24d042a83d0e
Source dataset
uspto-grants-1988_10
Patent number
US04775409

Reaction notes

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