Sodium Bicarbonate → (2-(2-Nitro-5-(piperidin-1-yl)phenyl)pyridin-4-yl)(3-(trifluoromethyl)phenyl)methanol

HRID 1408004Notes

Reaction equation

[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)=[CH:6][C:5]=1[C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][N:23]=1)[CH:19]=[O:20])([O-:3])=[O:2].[F:24][C:25]([F:35])([F:34])[C:26]1[CH:27]=[C:28]([Mg]Cl)[CH:29]=[CH:30][CH:31]=1.C([O-])(O)=O.[Na+]>C1COCC1>[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)=[CH:6][C:5]=1[C:16]1[CH:17]=[C:18]([CH:19]([C:30]2[CH:29]=[CH:28][CH:27]=[C:26]([C:25]([F:35])([F:34])[F:24])[CH:31]=2)[OH:20])[CH:21]=[CH:22][N:23]=1)([O-:3])=[O:2]

Participants

Conditions

Temperature: 0 °C

Procedure

To a −78° solution of 110 mg of 2-(2-nitro-5-(piperidin-1-yl)phenyl)isonicotinaldehyde in 4 mL of THF was added 0.82 mL of a 1.0 M solution of 3-(trifluoromethyl)phenylmagnesium chloride in THF. After 5 min the solution was warmed to 0° C. and treated with 10 mL of a saturated aqueous solution of NaHCO3. The mixture was extracted with ethyl acetate and the organic extracts were washed with water and then with brine. The solution was dried (Na2SO4) and the solvent was evaporated. The residue was purified by silica gel chromatography eluting with 1:1 ethyl acetate/hexanes to give 123 mg of product. MS (ES, m/z) 458.2 [M+H]+.

Workup

extractionThe mixture was extracted with ethyl acetate
washthe organic extracts were washed with water
dry with materialThe solution was dried (Na2SO4)
customthe solvent was evaporated
customThe residue was purified by silica gel chromatography
washeluting with 1:1 ethyl acetate/hexanes

Sources & evidence

ORD record: ord-c3f9e2df443a46c89ac9055567b04e9e
Source dataset: uspto-grants-2014_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08916569B2

Reaction notes

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