Dimethyl Sulfate → HCID 54044700, compound

HRID 2419308Notes

Reaction equation

HRID 2419308 reaction equation
[C:1]([NH:4][N:5]1[CH:9]=[N:8][N:7]=[C:6]1[N:10]([C:21](=[O:23])[CH3:22])[N:11]=[CH:12][C:13]1[C:18]([Cl:19])=[CH:17][CH:16]=[CH:15][C:14]=1[Cl:20])(=[O:3])[CH3:2].[C:24](=O)([O-])[O-].[Na+].[Na+].S(OC)(OC)(=O)=O>O>[CH3:24][N:4]([N:5]1[CH:9]=[N:8][N:7]=[C:6]1[N:10]([C:21](=[O:23])[CH3:22])[N:11]=[CH:12][C:13]1[C:14]([Cl:20])=[CH:15][CH:16]=[CH:17][C:18]=1[Cl:19])[C:1](=[O:3])[CH3:2]

Participants

5

Procedure

To a solution of 31.5 g of 4-acetamido-3-[1-acetyl-2-(2,6-dichlorobenzylidene) hydrazino]-1,2,4-triazole and 53.0 g of sodium carbonate in 400 ml of water is added dropwise, while stirring and cooling in an ice bath, 40 ml of dimethyl sulphate (2 h). After the addition the mixture was stirred for 2.5 h while cooling in ice and left overnight at room temperature. The obtained precipitate is collected and recrystallized twice from dioxane-isopropyl ether.

Workup

  1. temperaturecooling in an ice bath
  2. additionAfter the addition the mixture
  3. stirringwas stirred for 2.5 h
  4. temperaturewhile cooling in ice
  5. customThe obtained precipitate is collected
  6. customrecrystallized twice from dioxane-isopropyl ether

Sources & evidence

ORD record
ord-3358776fb5df45d381915d0a6faf1265
Source dataset
uspto-grants-1978_08
Patent number
US04105768

Reaction notes

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