Acetic Acid → HCID 178467936, compound

HRID 408532Notes

Reaction equation

HRID 408532 reaction equation
[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([CH:11]=O)[CH:9]=2)[NH:4][N:3]=1.[C:13](/[CH:15]=[C:16](\[O-:18])/[CH3:17])#[N:14].[Na+].C(O)(=O)C.N1CCCCC1>ClCCl>[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8](/[CH:11]=[C:15](/[C:16](=[O:18])[CH3:17])\[C:13]#[N:14])[CH:9]=2)[NH:4][N:3]=1

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 8082PiperidineHCID 23687916sodium (1Z)-1-cyanoprop-1-en-2-olateHCID 178434286HCID 178434286, compound

Product 1

HCID 178467936HCID 178467936, compoundYield 50%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A mixture of 5.0 g (31.2 mmol) 3-methyl-1H-indazole-5-carbaldehyde (Example 1A), 3.61 g (34.3 mmol) sodium (1Z)-1-cyanoprop-1-en-2-olate, 2.23 ml (39 mmol) acetic acid and 0.31 ml (3.12 mmol) piperidine in dry dichloromethane (250 ml) containing 4 Å molecular sieve was stirred under reflux for 12 h. Upon cooling, a precipitate was formed which was collected by filtration and washed with saturated aqueous sodium bicarbonate solution and water. The solid was dissolved in ethanol, and the molecular sieve was filtered off. The filtrate was concentrated under reduced pressure, and the residue was treated with ethyl acetate and saturated aqueous sodium carbonate solution. The organic layer was washed with water, dried, and concentrated under reduced pressure to afford the title compound (3.5 g, 50% of th.) as a pale yellow solid which was used in the next step without further purification.

Workup

  1. additioncontaining 4 Å molecular sieve
  2. temperatureunder reflux for 12 h
  3. temperatureUpon cooling
  4. customa precipitate was formed which
  5. filtrationwas collected by filtration
  6. washwashed with saturated aqueous sodium bicarbonate solution and water
  7. dissolutionThe solid was dissolved in ethanol
  8. filtrationthe molecular sieve was filtered off
  9. concentrationThe filtrate was concentrated under reduced pressure
  10. additionthe residue was treated with ethyl acetate and saturated aqueous sodium carbonate solution
  11. washThe organic layer was washed with water
  12. customdried
  13. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-2038f7827e3945fbad9e3409a21ce3d0
Source dataset
uspto-grants-2014_06
Patent number
US08759341B2

Reaction notes

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