Potassium Carbonate → HCID 9950049, compound

HRID 377644Notes

Reaction equation

HRID 377644 reaction equation
[NH2:1][C:2]1[N:6]([C:7]2[C:12]([Cl:13])=[CH:11][C:10]([C:14]([F:17])([F:16])[F:15])=[CH:9][C:8]=2[Cl:18])[N:5]=[C:4]([C:19]#[N:20])[C:3]=1[C:21]#[C:22][Si](C)(C)C.C(=O)([O-])[O-].[K+].[K+]>CO>[NH2:1][C:2]1[N:6]([C:7]2[C:8]([Cl:18])=[CH:9][C:10]([C:14]([F:15])([F:17])[F:16])=[CH:11][C:12]=2[Cl:13])[N:5]=[C:4]([C:19]#[N:20])[C:3]=1[C:21]#[CH:22]

Participants

4

Procedure

To a stirred solution of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trimethylsilylethynylpyrazole (2.0 g, crude from example 2) in methanol (30 ml) was added potassium carbonate (1 g). After 10 minutes at room temperature the reaction mixture was partitioned between ether (100 ml) and water (100 ml). The organic layer was separated, washed with brine (100 ml), dried (MgSO4) and evaporated. The residue was purified by column chromatography on silica gel eluted with dichloromethane followed by recrystallisation from ether to provide the title compound as a white solid, m.p. 215-216° C.

Workup

  1. customAfter 10 minutes at room temperature the reaction mixture was partitioned between ether (100 ml) and water (100 ml)
  2. customThe organic layer was separated
  3. washwashed with brine (100 ml)
  4. dry with materialdried (MgSO4)
  5. customevaporated
  6. customThe residue was purified by column chromatography on silica gel
  7. washeluted with dichloromethane
  8. customfollowed by recrystallisation from ether

Sources & evidence

ORD record
ord-d6ed17eebc044521b50cd699c23e2eb6
Source dataset
uspto-grants-2000_02
Patent number
US06028096

Reaction notes

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