Sodium Bicarbonate → N-(4-(4-benzyl-2,6-dimethylphenyl)thiazol-2-yl)isonicotinamide

HRID 1843815Notes

Reaction equation

HRID 1843815 reaction equation
[Br-].[CH2:2]([Zn+])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.I[C:11]1[CH:16]=[C:15]([CH3:17])[C:14]([C:18]2[N:19]=[C:20]([NH:23][C:24](=[O:31])[C:25]3[CH:30]=[CH:29][N:28]=[CH:27][CH:26]=3)[S:21][CH:22]=2)=[C:13]([CH3:32])[CH:12]=1.C([O-])(O)=O.[Na+]>C1COCC1>[CH2:2]([C:11]1[CH:12]=[C:13]([CH3:32])[C:14]([C:18]2[N:19]=[C:20]([NH:23][C:24](=[O:31])[C:25]3[CH:26]=[CH:27][N:28]=[CH:29][CH:30]=3)[S:21][CH:22]=2)=[C:15]([CH3:17])[CH:16]=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

Participants

5

Procedure

A THF solution of benzylzinc(II) bromide (4.0 mL, 2.0 mmol) was added to a degassed solution of N-(4-(4-iodo-2,6-dimethylphenyl)thiazol-2-yl)isonicotinamide (435 mg, 1.0 mmol) and tetrakistriphenylphosphine palladium (57.8 mg, 0.10 mmol) in THF (5.0 mL). The reaction mixture was heated at reflux for 16 h under N2 and then poured into saturated aqueous NaHCO3. The mixture was extracted with ethyl acetate, washed with brine, dried MgSO4, and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel to give N-(4-(4-benzyl-2,6-dimethylphenyl)thiazol-2-yl)isonicotinamide: 1H NMR (500 MHz, CDCl3) δ 8.70 (d, J=4.9 Hz, 2 H), 7.67 (d, J=4.9 Hz, 2 H), 7.33 (d, J=8.6 Hz, 2 H), 7.10-7.26 (m, 3 H), 6.80 (s, 1H), 6.24 (s, 1 H), 3.86 (s, 2 H), 2.04 (s, 6 H); ESI-MS: m/z 399.9 (M+H)+.

Workup

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 16 h under N2
  3. extractionThe mixture was extracted with ethyl acetate
  4. washwashed with brine, dried MgSO4
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by flash column chromatography on silica gel

Sources & evidence

ORD record
ord-b9f481d260214ed0901f63d7732cfdd1
Source dataset
uspto-grants-2015_02
Patent number
US08946268B2

Reaction notes

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