Ethyl Acetate → N-(4-(2-Aminopyridin-4-yloxy)-3-fluorophenyl)-2-(4-fluorophenylamino)isonicotinamide

HRID 1670272Notes

Reaction equation

HRID 1670272 reaction equation
C(OC1C=[CH:13][C:12]([NH:15][C:16]2[N:21]=CN=[C:18]([O:22][C:23]3[CH:28]=[CH:27][C:26]([NH:29][C:30](=[O:42])[CH2:31][C:32](NC4C=CC(F)=CC=4)=O)=[CH:25][C:24]=3[F:43])[CH:17]=2)=CC=1)C1C=CC=CC=1.CCO[C:47]([CH3:49])=O.C([O-])(O)=O.[Na+]>ClCCCl>[NH2:21][C:16]1[CH:17]=[C:18]([O:22][C:23]2[CH:28]=[CH:27][C:26]([NH:29][C:30](=[O:42])[C:31]3[CH:32]=[CH:12][N:15]=[C:16]([NH:21][C:47]4[CH:49]=[CH:25][C:24]([F:43])=[CH:23][CH:28]=4)[CH:17]=3)=[CH:25][C:24]=2[F:43])[CH:13]=[CH:12][N:15]=1

Participants

5

Reactant 3

HCID 8857Ethyl AcetateHCID 516892Sodium BicarbonateHCID 59853038N-(4-(6-(4-(Benzyloxy)phenylamino)pyrimidin-4-yloxy)-3-fluorophenyl)-N3-(4-fluorophenyl)malonamide2×

Product 1

HCID 46851683N-(4-(2-Aminopyridin-4-yloxy)-3-fluorophenyl)-2-(4-fluorophenylamino)isonicotinamideYield 6.3%

Reagents, catalysts & solvents 1

HCID 111,2-DichloroethaneSolvent2×

Procedure

A solution of 4-(4-amino-2-fluorophenoxy)pyridine-2-amine (Compound B of Example 24, 450 mg, 2.1 mmol) in 1,2-dichloroethane (10 mL) was added slowly to a solution of acylchloride obtained above in 1,2-dichloroethane (10 mL) at ice bath temperature with stirring. The reaction mixture was allowed to stand at rt overnight. To the reaction mixture were added EtOAc (150 mL) and saturated aq. NaHCO3 solution (50 mL). The EtOAc layer was separated, dried over MgSO4 and concentrated in vacuo. The residue was purified by preparative HPLC to obtain the title compound (69 mg, 6.3%) as a yellow solid (bis-TFA salt). 1H NMR (DMSO-d6) δ 10.90 (s, 1H), 9.32 (s, 1H), 8.27 (d, 1H, J=5.5 Hz), 7.92-7.07 (m, 11H), 6.68 (dd, 1H, J=7.1, 2.2 Hz), 6.10 (d, 1H, J=2.2 Hz); MS (ESI+) m/z 217.9 (M+H)+.

Workup

  1. customThe EtOAc layer was separated
  2. dry with materialdried over MgSO4
  3. concentrationconcentrated in vacuo
  4. customThe residue was purified by preparative HPLC

Sources & evidence

ORD record
ord-1cd0ec031eaf4f1380e74da61997c1d1
Source dataset
uspto-grants-2011_08
Patent number
US07989477B2

Reaction notes

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