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4-Amino-5-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one → HCID 14677257, compound

HRID 847468
Notes
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Reaction equation

HRID 847468 reaction equation
[NH2:1][N:2]1[C:6]([CH3:7])=[N:5][NH:4][C:3]1=[O:8].[F:9][C:10]([F:23])([F:22])[O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[S:18](Cl)(=[O:20])=[O:19]>N1C=CC=CC=1>[F:23][C:10]([F:9])([F:22])[O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[S:18]([NH:1][N:2]1[C:6]([CH3:7])=[N:5][NH:4][C:3]1=[O:8])(=[O:20])=[O:19]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 5750024-Amino-5-methyl-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 27772152-(Trifluoromethoxy)benzene-1-sulfonyl chloride

Product 1

HCID 14677257HCID 14677257, compoundYield 80%

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Conditions

Temperature
-10 °C

Procedure

10.0 g (0.088 mol) of 4-amino-5-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one are dissolved in 50 ml of dry pyridine, the mixture is cooled to -10° C., and 32.7 g (0.12 mol) of 2-trifluoromethoxy-benzenesulphonyl chloride are added. The reaction mixture is allowed to reach room temperature (approximately 20° C.) and stirred for approximately 12 hours. After the mixture has been concentrated, the residue is taken up in methylene chloride and shaken with 1N hydrochloric acid and then with water. The organic phase is dried with sodium sulfate and filtered. The solvent is carefully distilled off from the filtrate under a water pump vacuum. 23.1 g (80% of theory) of 4-(2-trifluoromethoxy-phenylsulphonylamino)-5-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one are obtained as an oily residue.

Workup

  1. customto reach room temperature
  2. custom(approximately 20° C.)
  3. concentrationAfter the mixture has been concentrated
  4. stirringshaken with 1N hydrochloric acid
  5. dry with materialThe organic phase is dried with sodium sulfate
  6. filtrationfiltered
  7. distillationThe solvent is carefully distilled off from the filtrate under a water pump vacuum

Sources & evidence

ORD record
ord-01560cbef84b4a6883d5370c1e39113a
Source dataset
uspto-grants-1992_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05142060

Reaction notes

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