Trifluoroacetic acid → 4-[[3-(2-Amino-5-chloro-3-pyridinyl)-5-isoxazolyl]methyl]phenol

HRID 640481Notes

Reaction equation

HRID 640481 reaction equation
FC(F)(F)C(O)=O.C([O:15][C:16]1[CH:35]=[CH:34][C:19]([CH2:20][C:21]2[O:25][N:24]=[C:23]([C:26]3[C:27]([NH2:33])=[N:28][CH:29]=[C:30]([Cl:32])[CH:31]=3)[CH:22]=2)=[CH:18][CH:17]=1)C1C=CC=CC=1.C1(SC)C=CC=CC=1.C(=O)([O-])O.[Na+]>O>[NH2:33][C:27]1[C:26]([C:23]2[CH:22]=[C:21]([CH2:20][C:19]3[CH:34]=[CH:35][C:16]([OH:15])=[CH:17][CH:18]=3)[O:25][N:24]=2)=[CH:31][C:30]([Cl:32])=[CH:29][N:28]=1

Participants

6

Reactant 4

HCID 6422Trifluoroacetic acidHCID 7520ThioanisoleHCID 516892Sodium BicarbonateHCID 59255519HCID 59255519, compound

Product 1

HCID 592555114-[[3-(2-Amino-5-chloro-3-pyridinyl)-5-isoxazolyl]methyl]phenolYield 62.4%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To a trifluoroacetic acid (6 mL) solution of 3-(5-(4-benzyloxy-benzyl)-isoxazol-3-yl)-5-chloro-pyridin-2-ylamine (304 mg, 0.776 mmol) described in Manufacturing Example 29-2-3 was added thioanisole (364 mL, 3.10 mmol) at 0° C., which was stirred for 3 hours at room temperature. To this reaction mixture were added sodium hydrogencarbonate and water at 0° C., which was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by NH silica gel column chromatography (ethyl acetate:methanol=20:1) to obtain the title compound (146 mg, 62%).

Workup

  1. extractionwhich was extracted with ethyl acetate
  2. customThe organic layer was separated
  3. washwashed with water and saturated aqueous sodium chloride
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationThe filtrate was concentrated under a reduced pressure
  7. customthe residue was purified by NH silica gel column chromatography (ethyl acetate:methanol=20:1)

Sources & evidence

ORD record
ord-10a03bab1e744acba6e8d0fc57f2de51
Source dataset
uspto-grants-2010_04
Patent number
US07691882B2

Reaction notes

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