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Potassium Carbonate → HCID 178497363, compound

HRID 1487819
Notes
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Reaction equation

HRID 1487819 reaction equation
Br[CH:2]([CH3:17])[C:3]([C:5]1[C:6]([CH3:16])=[CH:7][C:8]([CH3:15])=[C:9]([CH:14]=1)[C:10]([O:12][CH3:13])=[O:11])=O.Cl.[C:19](=[NH:22])([NH2:21])[CH3:20].C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[CH3:20][C:19]1[NH:21][C:3]([C:5]2[C:6]([CH3:16])=[CH:7][C:8]([CH3:15])=[C:9]([CH:14]=2)[C:10]([O:12][CH3:13])=[O:11])=[C:2]([CH3:17])[N:22]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 67170Acetamidine monohydrochlorideHCID 90021223Methyl 5-(2-bromopropanoyl)-2,4-dimethylbenzoate2×

Product 1

HCID 178497363HCID 178497363, compoundYield 58%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Conditions

Temperature
80 °C

Procedure

Into a round-bottom flask, was placed a solution of methyl 5-(2-bromopropanoyl)-2,4-dimethylbenzoate (compound 1.6, 400 mg, 1.34 mmol) in acetonitrile (30 mL). Acetimidamide hydrochloride (260 mg, 2.75 mmol) and potassium carbonate (550 mg, 3.99 mmol) were added and the resulting mixture was stirred at 80° C. for 15 h. After cooling to room temperature, the mixture was concentrated under reduced pressure and the residue was diluted with ethyl acetate (50 mL) and washed with brine (2×25 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with ethyl acetate/petroleum ether (1:1) to ethyl acetate as the eluent to yield the title compound as a yellow oil (0.20 g, 58%).

Workup

  1. customInto a round-bottom flask, was placed
  2. temperatureAfter cooling to room temperature
  3. concentrationthe mixture was concentrated under reduced pressure
  4. additionthe residue was diluted with ethyl acetate (50 mL)
  5. washwashed with brine (2×25 mL)
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by silica gel column chromatography with ethyl acetate/petroleum ether (1:1) to ethyl acetate as the eluent

Sources & evidence

ORD record
ord-552a72d8e85c447b9021220b8bb1cdb3
Source dataset
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09428502B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes