Sodium Methoxide → HCID 14032654, compound

HRID 986169Notes

Reaction equation

HRID 986169 reaction equation
[C:1]1([N:7]2[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[C:9]([CH:16]3[CH2:21][CH2:20][N:19]([C:22]#[N:23])[CH2:18][CH2:17]3)=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:24][O-:25].[Na+]>CO>[CH3:24][O:25][C:22]([N:19]1[CH2:18][CH2:17][CH:16]([C:9]2[C:10]3[C:15](=[CH:14][CH:13]=[CH:12][CH:11]=3)[N:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[N:8]=2)[CH2:21][CH2:20]1)=[NH:23]

Participants

4

Reactant 2

HCID 10942334Sodium MethoxideHCID 14032637HCID 14032637, compound

Product 1

HCID 14032654HCID 14032654, compoundYield 80.5%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A mixture of 4-(1-phenyl-1H-indazol-3-yl)piperidine-1-carbonitrile of Example 73 (4.0 g, 0.013 moles) and sodium methoxide (3 ml of 25% sodium methoxide in methanol, 0.013 moles) in methanol (30 ml) was warmed to effect solution and then stirred at ambient temperature for 16 hours. The solvent was removed which left an oil (4.5 g). The oil was dissolved in ether, washed with H2O, and dried (MgSO4). Removal of the ether left an oil which began to crystallize upon standing. Crystallization was enhanced by triturating the oil with hexane which produced 3.5 g of product. The product was recrystallized twice from hexane yielding 2.31 g (52%) of 4-(1-phenyl-1H-indazol-3-yl)piperidine-1-carboximidic acid methyl ester, mp 80°-83° C.

Workup

  1. temperaturewas warmed
  2. customThe solvent was removed which
  3. waitleft an oil (4.5 g)
  4. dissolutionThe oil was dissolved in ether
  5. washwashed with H2O
  6. dry with materialdried (MgSO4)
  7. customRemoval of the ether
  8. waitleft an oil which
  9. customto crystallize
  10. customCrystallization
  11. customby triturating the oil with hexane which

Sources & evidence

ORD record
ord-d8d7f0c7ef4e4b2c8abf2da39eef7230
Source dataset
uspto-grants-1987_12
Patent number
US04710573

Reaction notes

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