Methyl iodide → HCID 19075453, compound

HRID 1289676Notes

Reaction equation

HRID 1289676 reaction equation
[CH3:1][I:2].[CH2:3]([O:6][C:7]1[C:11]([C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)=[N:10][S:9][N:8]=1)[CH:4]=[CH2:5]>CC(C)=O>[I-:2].[CH2:3]([O:6][C:7]1[C:11]([C:12]2[CH:13]=[N+:14]([CH3:1])[CH:15]=[CH:16][CH:17]=2)=[N:10][S:9][N:8]=1)[CH:4]=[CH2:5]

Participants

4

Reactant 2

HCID 6328Methyl iodideHCID 19075381HCID 19075381, compound

Product 1

HCID 19075453HCID 19075453, compound

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

A mixture of methyl iodide (0.4 ml, 6 mmol) and 3-(3-(2-propenyloxy)-1,2,5-thiadiazol-4-yl)pyridine (3 mmol) in acetone (5 ml) was stirred at room temperature for 18 h. The title compound precipitiated from the solution and was collected by filtration to give 0.96 g (88%).

Workup

  1. filtrationThe title compound precipitiated from the solution and was collected by filtration
  2. customto give 0.96 g (88%)

Sources & evidence

ORD record
ord-fa27e35ceaa844d6822297cb5db314a9
Source dataset
uspto-grants-1998_05
Patent number
US05750541

Reaction notes

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