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Acetic Anhydride → 7-(2,4-dichloro-phenyl)-1H-pyrazolo[3,4-c]pyridine

HRID 902542
Notes
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Reaction equation

HRID 902542 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1[C:14]([NH:15]C(=O)C)=[C:13]([CH3:19])[CH:12]=[CH:11][N:10]=1.C(OC(=O)C)(=O)C.C([O-])(=O)C.[K+].[N:32](OCCC(C)C)=O.O.[OH-].[Li+]>O.C(O)C.C1C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1[N:10]=[CH:11][CH:12]=[C:13]2[CH:19]=[N:32][NH:15][C:14]=12
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

9

Reactant 5

HCID 7918Acetic AnhydrideHCID 8053Isoamyl NitriteHCID 168937Lithium hydroxide, monohydrateHCID 517044Potassium AcetateHCID 68614099N-[2-(2,4-dichloro-phenyl)4-methyl-pyridin-3-yl]-acetamide

Product 1

HCID 686152427-(2,4-dichloro-phenyl)-1H-pyrazolo[3,4-c]pyridine
Yield 68.6%

Reagents, catalysts & solvents 3

HCID 241BenzeneSolventHCID 702EthanolSolventHCID 962WaterSolvent

Procedure

To a mixture of N-[2-(2,4-dichloro-phenyl)-4-methyl-pyridin-3-yl]-acetamide (30; 0.787 g, 2.67 mmol), 30 mL of benzene, acetic anhydride (0.780 mL, 8.27 mmol), and potassium acetate (0.330 g, 3.36 mmol) at 78° C. was added isoamyl nitrite (0.572 mL, 4.27 mmol), and the yellow mixture was stirred for 22 h. After cooling, the mixture was filtered and concentrated to an orange oil. To the oil was added 21 mL of ethanol, 7 mL of water, and lithium hydroxide monohydrate (0.339 g, 8.80 mmol). The orange mixture was stirred for 3 h, then concentrated to remove ethanol. The orange residue was partitioned between 50 mL of diethyl ether and 50 mL of a 10% aqueous NaOH solution, and the aqueous layer was extracted with 50 mL of diethyl ether. The combined organic layers were washed with 100 mL of a saturated aqueous NaCl solution, dried over MgSO4, filtered, loaded onto silica gel and concentrated. Column chromatography (0→20% EtOAc/hexanes) afforded of 7-(2,4-dichloro-phenyl)-1H-pyrazolo[3,4-c]pyridine (31; 0.484 g; 67%) as a foamy pale yellow solid.

Workup

  1. temperatureAfter cooling
  2. filtrationthe mixture was filtered
  3. concentrationconcentrated to an orange oil
  4. stirringThe orange mixture was stirred for 3 h
  5. concentrationconcentrated
  6. customto remove ethanol
  7. customThe orange residue was partitioned between 50 mL of diethyl ether and 50 mL of a 10% aqueous NaOH solution
  8. extractionthe aqueous layer was extracted with 50 mL of diethyl ether
  9. washThe combined organic layers were washed with 100 mL of a saturated aqueous NaCl solution
  10. dry with materialdried over MgSO4
  11. filtrationfiltered
  12. concentrationconcentrated

Sources & evidence

ORD record
ord-0edab7bcbfbc462e9edcc05eb5f305f9
Source dataset
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07365211B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes