Ammonia → 6-Chloro-5-(1H-imidazol-2-yl)-N-(4-(trifluoromethoxy)phenyl)nicotinamide

HRID 629107Notes

Reaction equation

HRID 629107 reaction equation
[CH:1]([Mg]Cl)([CH3:3])C.[Cl:6][C:7]1[C:26](I)=[CH:25][C:10]([C:11]([NH:13][C:14]2[CH:19]=[CH:18][C:17]([O:20][C:21]([F:24])([F:23])[F:22])=[CH:16][CH:15]=2)=[O:12])=[CH:9][N:8]=1.C[N:29]([CH:31]=O)C.[NH4+:33].[Cl-].C(C=O)=O.O.N>C1COCC1>[Cl:6][C:7]1[C:26]([C:31]2[NH:29][CH:1]=[CH:3][N:33]=2)=[CH:25][C:10]([C:11]([NH:13][C:14]2[CH:19]=[CH:18][C:17]([O:20][C:21]([F:24])([F:23])[F:22])=[CH:16][CH:15]=2)=[O:12])=[CH:9][N:8]=1

Participants

9

Reactant 7

HCID 222AmmoniaHCID 962WaterHCID 6228DimethylformamideHCID 7860GlyoxalHCID 25517Ammonium ChlorideHCID 867025996-chloro-5-iodo-N-(4-(trifluoromethoxy)phenyl)nicotinamideHCID 178418918HCID 178418918, compound

Product 1

HCID 722014366-Chloro-5-(1H-imidazol-2-yl)-N-(4-(trifluoromethoxy)phenyl)nicotinamide

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
-75 °C

Procedure

A solution of isopropyl magnesium chloride 2 M in THF (2.5 mL, 5 mmol) was added dropwise to a solution of 6-chloro-5-iodo-N-(4-(trifluoromethoxy)phenyl)nicotinamide (Stage 65.1, 885 mg, 2 mmol) in THF (15 mL) at a temperature between −70 and −85° C. under an argon atmosphere. The RM was then stirred at between −45 and −40° C. for 30 min, then cooled to −75° C. and treated dropwise with DMF (0.465 mL, 6.00 mmol). The RM allowed to slowly warm to RT, then treated with NH4Cl aq. solution (15 mL) and extracted with EtOAc. The combined extracts were washed with a sat. NH4Cl solution, with water and brine, dried over MgSO4 and the solvent was evaporated off under reduced pressure. The residue was dissolved in MeOH (10 mL), treated with glyoxal 40% in water (0.178 mL, 3.89 mmol) and 25% aq. NH3 (1.462 mL, 19.44 mmol) and the RM was stirred for at RT for 24 h. The solvent was evaporated off under reduced pressure and the residue was treated with water and extracted with EtOAc. The combined extracts were washed with water and brine, dried over Na2SO4 and the solvent was evaporated off under reduced pressure to give the crude product which was purified by column chromatography (Silica gel, 50 g, n-hexane/EtOAc 2:1 and 1:1) and recrystallized from n-hexane/EtOAC to afford the title product as white crystals. UPLC-MS (Condition 2) tR 0.88 min, m/z=383.1 [M+H]+; 1H-NMR (600 MHz, DMSO-d6) δ ppm 7.19 (s, 1H) 7.41 (d, J=7.72 Hz, 3H) 7.89 (d, J=8.85 Hz, 2H) 8.76 (d, J=2.07 Hz, 1H) 8.94 (d, J=2.07 Hz, 1H) 10.77 (s, 1H) 12.60 (br. s, 1H).

Workup

  1. temperatureto slowly warm to RT
  2. extractionextracted with EtOAc
  3. washThe combined extracts were washed with a sat. NH4Cl solution, with water and brine
  4. dry with materialdried over MgSO4
  5. customthe solvent was evaporated off under reduced pressure
  6. dissolutionThe residue was dissolved in MeOH (10 mL)
  7. stirringthe RM was stirred for at RT for 24 h
  8. customThe solvent was evaporated off under reduced pressure
  9. additionthe residue was treated with water
  10. extractionextracted with EtOAc
  11. washThe combined extracts were washed with water and brine
  12. dry with materialdried over Na2SO4
  13. customthe solvent was evaporated off under reduced pressure
  14. customto give the crude product which
  15. customwas purified by column chromatography (Silica gel, 50 g, n-hexane/EtOAc 2:1 and 1:1)
  16. customrecrystallized from n-hexane/EtOAC

Sources & evidence

ORD record
ord-b6d9880daef64f35898e7dd8e7e223f4
Source dataset
uspto-grants-2016_04
Patent number
US09315489B2

Reaction notes

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