Reaction #474624

ord-5e0cd5dc6fb64b34a4ef439141bb4c13

Reaction equation

O=C([O-])[O-].[K+].[K+]
K2CO3
C[Si](C)(C)[N-][Si](C)(C)C.[K+]
potassium bis(trimethylsilyl)amide
Oc1ccc(-c2nnc(Nc3ccc(OC(F)(F)F)cc3)[nH]2)cc1
4-[5-(4-trifluoromethoxy-phenylamino)-4H[1,2,4]triazol-3-yl]-phenol
NC(=O)c1cc(Cl)ccn1
4-chloro-2-pyridinecarboxamide
CNC(=O)c1cc(Oc2ccc(-c3nnc(Nc4ccc(OC(F)(F)F)cc4)[nH]3)cc2)ccn1.O=C(O)C(F)(F)F
TFA
Yield 40.5%
CNC(=O)c1cc(Oc2ccc(-c3nnc(Nc4ccc(OC(F)(F)F)cc4)[nH]3)cc2)ccn1.O=C(O)C(F)(F)F
4-{4-[5-(4-trifluoromethoxy-phenylamino)-4H-[1,2,4]triazol-3-yl]-phenoxy}-pyridine-2-carboxylic acid methylamide trifluoroacetic acid salt
Yield 40.5%

Solvents

Conditions

Temperature
80°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherThen the vial was capped
  2. 2
    Othermicrowaved at 200° C. for 15 min
  3. 3
    Filtrationfiltered through 0.22 um syringe
  4. 4
    Filtrationfilter
  5. 5
    Otherpurified by reverse-phase preparative HPLC in acetonitrile/water system with 0.01% TFA

Procedure

4-[5-(4-trifluoromethoxy-phenylamino)-4H[1,2,4]triazol-3-yl]-phenol (66.4 mg, 0,197 mmol) was dissolved in 2 mL of anhydrous DMF in a 5 mL microwave vial (Personal Chemistry). Solid potassium bis(trimethylsilyl)amide (39.4 mg, 0.197 mmol) was added and the reaction mixture was stirred with heating at 80° C. for 15 min, then 4-chloro-2-pyridinecarboxamide (33.7 mg, 0.197 mmol) was added, followed by anhydrous K2CO3 (27.3 mg, 0.197 mmol). Then the vial was capped and microwaved at 200° C. for 15 min. Then the reaction mixture was diluted with ca. 1 mL of MeOH, filtered through 0.22 um syringe filter and purified by reverse-phase preparative HPLC in acetonitrile/water system with 0.01% TFA. The product was isolated as a TFA salt (46.6 mg).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08372971B2uspto-grants-2013_02