Methyl iodide → 3-(3-(2-(2-Methoxyethoxy)ethoxy)-1,2,5-thiadiazol-4-Yl)-1-methylpyridinium iodide

HRID 1975146Notes

Reaction equation

HRID 1975146 reaction equation
[CH3:1][I:2].[CH3:3][O:4][CH2:5][CH2:6][O:7][CH2:8][CH2:9][O:10][C:11]1[C:12]([C:16]2[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=2)=[N:13][S:14][N:15]=1>CC(C)=O>[I-:2].[CH3:3][O:4][CH2:5][CH2:6][O:7][CH2:8][CH2:9][O:10][C:11]1[C:12]([C:16]2[CH:17]=[N+:18]([CH3:1])[CH:19]=[CH:20][CH:21]=2)=[N:13][S:14][N:15]=1

Participants

4

Reactant 2

HCID 6328Methyl iodideHCID 19075261HCID 19075261, compound

Product 1

HCID 190752853-(3-(2-(2-Methoxyethoxy)ethoxy)-1,2,5-thiadiazol-4-Yl)-1-methylpyridinium iodide

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

A mixture of methyl iodide (0.5 ml, 9 mmol) and 3-(4-(2-(2-methoxyethoxy) ethoxy)-1,2,5-thiadiazol-3-yl)pyridine (3 mmol) in acetone (10 ml) was stirred at room temperature for 18 h. The title compound precipitated from the solution and was collected by filtration to yield 0.76 g (60%).

Workup

  1. customThe title compound precipitated from the solution
  2. filtrationwas collected by filtration
  3. customto yield 0.76 g (60%)

Sources & evidence

ORD record
ord-2ea2546f42b24271ae3f2ac84297ce7d
Source dataset
uspto-grants-1994_02
Patent number
US05284859

Reaction notes

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