Water → HCID 67235649, compound

HRID 1023587Notes

Reaction equation

HRID 1023587 reaction equation
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([O:10][C:11]2[CH:18]=[CH:17][C:14]([C:15]#[N:16])=[CH:13][C:12]=2[C:19]([F:22])([F:21])[F:20])=[N:8][CH:9]=1)([O-])=O.O.[NH4+].[Cl-]>C1COCC1.[Fe]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([O:10][C:11]2[CH:18]=[CH:17][C:14]([C:15]#[N:16])=[CH:13][C:12]=2[C:19]([F:22])([F:20])[F:21])=[N:8][CH:9]=1

Participants

6

Procedure

To a solution of 4-[(5-nitro-2-pyridinyl)oxy]-3-(trifluoromethyl)benzonitrile (Intermediate 120, 83 mg) in THF (3 mL)/water (1.5 mL) was added at room temperature, iron (75 mg, 1.34 mmol) and NH4Cl (72 mg, 1.34 mmol) and the resulting reaction mixture was stirred overnight. The mixture was filtered through a small pad of celite washing with EtOAc and water. To the filtered mixture was added an aqueous NaHCO3 saturated solution and the two phases were separated. The aqueous phase was extracted with EtOAc and the combined organic phases were dried and evaporated to dryness. The crude was purified by flash chromatography (companion system, 2×12 g Si cartridge, from 100:0 to 70:30 Cyclohexane/EtOAc) to afford the title compound (72 mg).

Workup

  1. filtrationThe mixture was filtered through a small pad of celite
  2. washwashing with EtOAc and water
  3. additionTo the filtered mixture was added an aqueous NaHCO3 saturated solution
  4. customthe two phases were separated
  5. extractionThe aqueous phase was extracted with EtOAc
  6. customthe combined organic phases were dried
  7. customevaporated to dryness
  8. customThe crude was purified by flash chromatography (companion system, 2×12 g Si cartridge, from 100:0 to 70:30 Cyclohexane/EtOAc)

Sources & evidence

ORD record
ord-04f9e727ebdc4291814218ee6f82c8df
Source dataset
uspto-grants-2014_05
Patent number
US08722695B2

Reaction notes

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