p-Toluenesulfonic acid monohydrate → HCID 15837816, compound

HRID 975308Notes

Reaction equation

HRID 975308 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]1[CH:14]=[CH:13][C:12]([CH2:15][NH:16][C:17]2[C:22]([NH:23][C:24]([CH:26]3[CH2:28][CH2:27]3)=O)=[C:21]([CH3:29])[C:20]([Br:30])=[CH:19][N:18]=2)=[CH:11][CH:10]=1)#[N:2].O.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[CH:26]1([C:24]2[N:16]([CH2:15][C:12]3[CH:13]=[CH:14][C:9]([C:4]4[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=4[C:1]#[N:2])=[CH:10][CH:11]=3)[C:17]3=[N:18][CH:19]=[C:20]([Br:30])[C:21]([CH3:29])=[C:22]3[N:23]=2)[CH2:28][CH2:27]1

Participants

4

Reactant 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 15837815HCID 15837815, compound

Product 1

HCID 15837816HCID 15837816, compoundYield 89.2%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

Toluene (20 ml) was added to 2.0 g (4.3 mmol) of 2-(2'-cyanobiphenyl-4-yl)methylamino-3-cyclopropanecarboxamido-5-bromo-4-methylpyridine, p-toluenesulfonic acid monohydrate (200 mg) and Molecular Sieves 4A (500 mg) followed by heating under reflux with stirring for 3 hours. The reaction solution was brought to room temperature and filtered through Celite to remove insolubles. Chloroform (100 ml) and an aqueous solution (100 ml) of sodium hydrogencarbonate were added to the flitrate and the obtained mixture was caused liquid-liquid separation. The aqueous phase was further extracted with chloroform (50 ml) twice. The organic phases were combined, dried over anhydrous magnesium sulfate an(subjected to vacuum concentration. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to give 1.7 g of 2-cyclopropyl-3-(2'-cyanobiphenyl-4-yl)methyl-6-bromo-7-methyl-3H-imidazo[4,5-b]pyridine (yield 88%).

Workup

  1. temperatureby heating
  2. temperatureunder reflux
  3. customwas brought to room temperature
  4. filtrationfiltered through Celite
  5. customto remove insolubles
  6. additionChloroform (100 ml) and an aqueous solution (100 ml) of sodium hydrogencarbonate were added to the flitrate
  7. customliquid-liquid separation
  8. extractionThe aqueous phase was further extracted with chloroform (50 ml) twice
  9. dry with materialdried over anhydrous magnesium sulfate
  10. concentrationan(subjected to vacuum concentration
  11. customThe residue was purified by silica gel column chromatography (n-hexane/ethyl acetate)

Sources & evidence

ORD record
ord-f1a14599d7d1459b8c7047359ed639d3
Source dataset
uspto-grants-1997_03
Patent number
US05608068

Reaction notes

Loading…