Sodium Hydroxide → 5-[2-(4-Methoxyphenyl)-ethyl]-1H-pyrazole-3-carboxylic acid

HRID 1724741Notes

Reaction equation

HRID 1724741 reaction equation
[OH-].[Na+].C([O:5][C:6]([C:8]1[CH:12]=[C:11]([CH2:13][CH2:14][C:15]2[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=2)[NH:10][N:9]=1)=[O:7])C>CO>[CH3:22][O:21][C:18]1[CH:19]=[CH:20][C:15]([CH2:14][CH2:13][C:11]2[NH:10][N:9]=[C:8]([C:6]([OH:7])=[O:5])[CH:12]=2)=[CH:16][CH:17]=1

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 57435076HCID 57435076, compound

Product 1

HCID 118452975-[2-(4-Methoxyphenyl)-ethyl]-1H-pyrazole-3-carboxylic acid

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Freshly prepared aq. NaOH (10 M in H2O, 25.4 mmol) was added to a stirring, room temperature solution of 23 (1.391 g, 5.07 mmol) in MeOH (12.7 mL, 0.4 M) under N2. The reaction was then heated to reflux until the reaction was judged complete by HPLC (30 min): The reaction was concentrated and then dissolved in 10 mL H2O. The reaction was extracted with a small amount of EtOAc, then the aqueous layer was made acidic (pH=2) with the dropwise addition of 10% aq. HCl. The white solid that precipitated from the reaction was filtered off and washed with cold H2O. The solid was dried under vacuum overnight to obtain 0.3771 g of relatively pure 24. 24 was further purified by recrystallization from warm MeOH to obtain 0.1317 g of pure 24. No attempts were made to recover remaining 24 from the mother liquor. 1H (CD3OD, 400 MHz): 7.07 (2H, d, J=8.2 Hz), 6.84 (2H, d, J=8.6 Hz), 6.53 (1H, s), 3.73 (3H, s), 2.97-2.84 (4H, m) ppm. 13C (CD3OD, 100 MHz): δ 164.86, 159.60, 148.26, 143.15, 134.01, 130.36, 114.81, 107.50, 55.60, 35.67, 29.10 ppm.

Workup

  1. temperatureThe reaction was then heated
  2. temperatureto reflux until the reaction
  3. customwas judged complete by HPLC (30 min)
  4. concentrationThe reaction was concentrated
  5. dissolutiondissolved in 10 mL H2O
  6. extractionThe reaction was extracted with a small amount of EtOAc
  7. additionwith the dropwise addition of 10% aq. HCl
  8. customThe white solid that precipitated from the reaction
  9. filtrationwas filtered off
  10. washwashed with cold H2O
  11. customThe solid was dried under vacuum overnight
  12. customto obtain 0.3771 g of relatively pure 24
  13. custom24 was further purified by recrystallization
  14. temperaturefrom warm MeOH
  15. customto obtain 0.1317 g of pure 24
  16. customto recover

Sources & evidence

ORD record
ord-5f9e3751b1664140a102561139d9f6b6
Source dataset
uspto-grants-2009_02
Patent number
US07488747B2

Reaction notes

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