Water → HCID 67235649, compound

HRID 527731Notes

Reaction equation

HRID 527731 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 (Reference Intermediate R13, 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-6d25978c76634c52a67ce666af12027f
Source dataset
uspto-grants-2016_05
Patent number
US09346790B2

Reaction notes

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