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Dimethyl Sulfate → 6-Bromo-2-methoxy-N-methyl-1-naphthamide

HRID 480452
Notes
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Reaction equation

HRID 480452 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([C:12]([NH:14][CH3:15])=[O:13])=[C:7]([OH:16])[CH:6]=[CH:5]2.[CH3:17]OS(OC)(=O)=O.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([C:12]([NH:14][CH3:15])=[O:13])=[C:7]([O:16][CH3:17])[CH:6]=[CH:5]2
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 187690866-Bromo-2-hydroxy-N-methyl-1-naphthamide

Product 1

HCID 187690686-Bromo-2-methoxy-N-methyl-1-naphthamide

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
60 °C

Procedure

A mixture of 6-Bromo-2-hydroxy-N-methyl-1-naphthamide (1.20 g), dimethylsulfate (0.49 mL), and powdered K2CO3 (1.18 g) in anhydrous DMF (10 mL) was heated at 60° C. for 30 min. After dilution with 1N HCl, the resulting mixture was extracted with Ethyl acetate. The combined organic layers were washed with water and brine followed by drying over MgSO4. After removal of the solvent in vacuo, the residue was washed with hexane-AcOEt (1:1) to give the title compound (1.21 g) as a colorless powder.

Workup

  1. extractionAfter dilution with 1N HCl, the resulting mixture was extracted with Ethyl acetate
  2. washThe combined organic layers were washed with water and brine
  3. dry with materialby drying over MgSO4
  4. customAfter removal of the solvent in vacuo
  5. washthe residue was washed with hexane-AcOEt (1:1)

Sources & evidence

ORD record
ord-a28776cc27d64c1197245c418599af5c
Source dataset
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06649643B1

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes