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Potassium Carbonate → 2-(Imidazo[1,2-a]pyridin-8-ylmethoxy)-5-methoxybenzaldehyde

HRID 1473887
Notes
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Reaction equation

HRID 1473887 reaction equation
Cl[CH2:2][C:3]1[C:4]2[N:5]([CH:9]=[CH:10][N:11]=2)[CH:6]=[CH:7][CH:8]=1.[OH:12][C:13]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:14]=1[CH:15]=[O:16].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[N:11]1[CH:10]=[CH:9][N:5]2[CH:6]=[CH:7][CH:8]=[C:3]([CH2:2][O:12][C:13]3[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:14]=3[CH:15]=[O:16])[C:4]=12
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 956952-Hydroxy-5-methoxybenzaldehydeHCID 216615828-(Chloromethyl)imidazo[1,2-a]pyridine

Product 1

HCID 716214602-(Imidazo[1,2-a]pyridin-8-ylmethoxy)-5-methoxybenzaldehydeYield 45%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
87.5 °C

Procedure

To a solution of the crude 8-(chloromethyl)imidazo[1,2-a]pyridine (6.8 mmol, 1 eq) and 2-hydroxy-5-methoxybenzaldehyde (1.3 g, 8.1 mmol, 1.2 eq) in DMF (20 mL) was added potassium carbonate (2.8 g, 20.4 mmol, 3 eq) and the reaction mixture was heated at 85-90° C. for 5 h. DMF was removed under vacuum and the residue was taken in ethyl acetate and filtered. The solid was washed with additional ethyl acetate, and then dried and evaporated to give the crude, which was purified by column chromatography (EtOAc/Hexane) to yield the desired compound in 45% yield. NMR (400 MHz, CDCl3): δ 3.80 (s, 3H), 5.60 (s, 2H), 6.85 (d, 1H), 7.12 (d, 2H), 7.36 (m, 2H), 7.66 (m, 2H), 8.14 (m, 1H), 10.58 (s, 1H); MS: exact mass calculated for C16H14N2O3, 282.10; m/z found, 283 [M+H]+.

Workup

  1. customDMF was removed under vacuum
  2. filtrationfiltered
  3. washThe solid was washed with additional ethyl acetate
  4. customdried
  5. customevaporated
  6. customto give the crude, which
  7. customwas purified by column chromatography (EtOAc/Hexane)

Sources & evidence

ORD record
ord-0eb5b9b6080743bdb70dd0e756544964
Source dataset
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09018210B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes