Bicarbonate Ion → HCID 22672578, compound

HRID 1006679Notes

Reaction equation

HRID 1006679 reaction equation
[CH3:1][C:2]1[N:3]=[C:4]2[C:9]([NH:10][CH2:11][C:12]3[C:17]([CH3:18])=[CH:16][CH:15]=[CH:14][C:13]=3[CH3:19])=[CH:8][C:7]([CH2:20][OH:21])=[CH:6][N:5]2[C:22]=1[CH3:23].S(Cl)([Cl:26])=O.[C:28](=O)(O)[O-]>C(Cl)Cl>[ClH:26].[CH3:1][C:2]1[N:3]=[C:4]2[C:9]([NH:10][CH2:11][C:12]3[C:13]([CH3:19])=[CH:14][CH:15]=[CH:16][C:17]=3[CH3:18])=[CH:8][C:7]([CH2:20][O:21][CH3:28])=[CH:6][N:5]2[C:22]=1[CH3:23]

Participants

5

Procedure

To a stirred solution of 2,3-dimethyl-8-(2,6-dimethylbenzylamino)-6-hydroxymethylimidazo[1,2-a]pyridine (0.08 g, 0.26 mmol) in methylene chloride (5 ml) was added thionyl chloride (0.038 ml, 0.52 mmol) and the mixture was stirred for 2 h. A saturated bicarbonate solution was added and the organic layer was separated, dried (Na2SO4) and evaporated under reduced pressure. To the residue was added methanol (5 ml) the mixture was stirred overnight. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography on silica gel using methylene chloride:methanol (100:5) as eluent. Treating the residue with HCl/diethyl ether and filtration gave 0.01 g (11%) of the title compound.

Workup

  1. customthe organic layer was separated
  2. dry with materialdried (Na2SO4)
  3. customevaporated under reduced pressure
  4. additionTo the residue was added methanol (5 ml) the mixture
  5. stirringwas stirred overnight
  6. customThe solvent was evaporated under reduced pressure
  7. customthe residue was purified by column chromatography on silica gel
  8. additionTreating the residue
  9. filtrationwith HCl/diethyl ether and filtration

Sources & evidence

ORD record
ord-9d2afb713df24b369becadbadc35146d
Source dataset
uspto-grants-2004_09
Patent number
US06790960B2

Reaction notes

Loading…