Water → ethyl 3-[(1E)-4-methoxybut-1-en-1-yl]imidazo[1,2-a]pyridine-2-carboxylate

HRID 1509531Notes

Reaction equation

HRID 1509531 reaction equation
[Br-].[CH3:2][O:3][CH2:4][CH2:5][CH2:6][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.CC(C)([O-])C.[K+].[CH:32]([C:34]1[N:38]2[CH:39]=[CH:40][CH:41]=[CH:42][C:37]2=[N:36][C:35]=1[C:43]([O:45][CH2:46][CH3:47])=[O:44])=O.O>C1COCC1>[CH3:2][O:3][CH2:4][CH2:5]/[CH:6]=[CH:32]/[C:34]1[N:38]2[CH:39]=[CH:40][CH:41]=[CH:42][C:37]2=[N:36][C:35]=1[C:43]([O:45][CH2:46][CH3:47])=[O:44]

Participants

6

Procedure

To a suspension of (3-methoxypropyl) (triphenyl)phosphonium bromide (3.56 g) in THF (50 ml) was added potassium tert-butoxide (0.38 g) at −78° C., and the mixture was stirred at the same temperature for 30 min. Ethyl 3-formylimidazo[1,2-a]pyridine-2-carboxylate (1.7 g) was added to the reaction mixture, and the mixture was stirred at room temperature for 12 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate was concentrated under reduced pressure to give the object product (256 mg).

Workup

  1. stirringthe mixture was stirred at room temperature for 12 hr
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe extract was washed with saturated brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. customThe solvent was evaporated under reduced pressure
  6. washa fraction eluted with ethyl acetate
  7. concentrationwas concentrated under reduced pressure

Sources & evidence

ORD record
ord-e574cc6a85834b4fba85b187fa81780f
Source dataset
uspto-grants-2015_12
Patent number
US09221836B2

Reaction notes

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