Sodium Hydroxide → 5-(Trifluoromethyl)-1,2,4-triazin-3-amine

HRID 1167112Notes

Reaction equation

HRID 1167112 reaction equation
O.O.O.C([O-])(=O)C.[Na+].Br[CH:10](Br)[C:11]([C:13]([F:16])([F:15])[F:14])=O.C(=O)(O)O.[NH2:22][NH:23][C:24]([NH2:26])=[NH:25].[OH-].[Na+]>O>[NH2:26][C:24]1[N:23]=[N:22][CH:10]=[C:11]([C:13]([F:16])([F:15])[F:14])[N:25]=1

Participants

6

Procedure

To a stirred solution of sodium acetate trihydrate (22.62 g, 166.2 mmol) in water (80 ml) was added 1,1-dibromo-3,3,3-trifluoroacetone (21.57 g, 79.9 mmol). The solution was heated at reflux under nitrogen for 30 min, then allowed to cool to room temperature before adding solid aminoguanidine bicarbonate (10.88 g, 79.9 mmol). The resulting pale yellow solution (pH 5) was stirred at room temperature for 3 h, then 4 N aqueous NaOH solution (40 ml, 160 mmol) was added causing a precipitate to appear. The mixture (pH 10) was stirred under nitrogen for a further 39 h. The solid was collected by filtration, washed with water and dried at 60° C. under vacuum to give 6.96 g of a mixture of two isomers in a 28:72 ratio. This was further purified by flash chromatography (silica gel, 30% EtOAc/isohexane), then recrystallised from ethanol to afford 3.53 g (27%) of the title compound: 1H NMR (400 MHz, DMSO-d6) δ 8.00 (2H, br s), 9.08 (1H, s).

Workup

  1. temperatureThe solution was heated
  2. temperatureat reflux under nitrogen for 30 min
  3. filtrationThe solid was collected by filtration
  4. washwashed with water
  5. customdried at 60° C. under vacuum

Sources & evidence

ORD record
ord-1c7584528bc54295b771c6db7b345374
Source dataset
uspto-grants-2003_09
Patent number
US06617326B2

Reaction notes

Loading…