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Methyl iodide → HCID 22174876, compound

HRID 1797139
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Reaction equation

HRID 1797139 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[N:12]=[CH:11][N:10]=[C:9]([SH:13])[N:8]=1.[C:14](=O)([O-])[O-].[Na+].[Na+].IC>CC(C)=O>[CH3:14][S:13][C:9]1[N:8]=[C:7]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=2)[N:12]=[CH:11][N:10]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 10340Sodium CarbonateHCID 178527892HCID 178527892, compound

Product 1

HCID 22174876HCID 22174876, compound

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

To a stirred suspension of the product of step 1 (0.707 g, 3.72 mmol) in acetone (36 mL) was added sodium carbonate (0.79 g, 7.5 mmol) followed by iodomethane (0.35 mL, 5.6 mmol). After overnight stirring, the reaction was filtered free of undissolved solid and concentrated to afford product as light brown solid: 1H NMR (DMSO-d6) δ 9.13 (s, 1H), 8.84–8.76 (m, 1H), 8.55–8.43 (m, 1H), 8.11–8.00 (m, 1H), 7.69–7.60 (m, 1H), 2.63 (s, 3H) ppm.

Workup

  1. filtrationthe reaction was filtered free of undissolved solid
  2. concentrationconcentrated
  3. customto afford product as light brown solid

Sources & evidence

ORD record
ord-0dc708d3d3ad4ba0856ae0336b210295
Source dataset
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07034031B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes