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Methyl iodide → HCID 848831, compound

HRID 443981
Notes
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Reaction equation

HRID 443981 reaction equation
[CH3:1][C:2]1[C:3](=[O:14])[NH:4][C:5]2[C:10]([N:11]=1)=[CH:9][C:8]([CH3:12])=[C:7]([CH3:13])[CH:6]=2.CI.[C:17](=O)([O-])[O-].[Na+].[Na+]>CN(C)C=O>[CH3:17][N:4]1[C:5]2[C:10](=[CH:9][C:8]([CH3:12])=[C:7]([CH3:13])[CH:6]=2)[N:11]=[C:2]([CH3:1])[C:3]1=[O:14]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 10340Sodium CarbonateHCID 2474892-Hydroxy-3,6,7-trimethylquinoxaline

Product 1

HCID 848831HCID 848831, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

A mixture of 3,6,7-trimethyl-2(1H)-quinoxalinone (5.0 g., 0.027 mol.), methyl iodide (15 ml.), sodium carbonate (5.0 g., 0.047 mol.) and dimethylformamide (75 ml.) was stirred at room temperature for eighteen hours, then heated at 75°-80° C. for three hours. Removal of the dimethylformamide under reduced pressure and dilution with water gave a brown solid. Crystallization from acetone (Darco) gave light tan needles. (2.85 g., m.p. 164°-166°, 53%)

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. temperatureheated at 75°-80° C. for three hours
  2. customRemoval of the dimethylformamide under reduced pressure and dilution with water
  3. customgave a brown solid
  4. customCrystallization from acetone (Darco)
  5. customgave light tan needles

Sources & evidence

ORD record
ord-bdf727b8224d438b9570ccfefa72075d
Source dataset
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04262123

Reaction notes

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