Guanidine Hydrochloride → HCID 178433869, compound

HRID 2298019Notes

Reaction equation

HRID 2298019 reaction equation
[ClH:1].[NH2:2][C:3]([NH2:5])=[NH:4].C[O-].[Na+].CN(C)C=O.[CH3:14][C:15]1[C:19]([C:20](OC)=[O:21])=[N:18][N:17]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[N:16]=1>CO.O.O1CCCC1>[ClH:1].[CH3:14][C:15]1[C:19]([C:20]([NH:4][C:3]([NH2:5])=[NH:2])=[O:21])=[N:18][N:17]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[N:16]=1

Participants

8

Conditions

Temperature
70 °C

Procedure

Guanidine hydrochloride (2.42 g, 25.32 mmol) was dissolved in 20 ml of anhydrous methanol and then treated with sodium methoxide (1.50 g, 27.83 mmol), added in one portion at room temperature. The reaction mixture was stirred under nitrogen for 1 hour, then filtered under a nitrogen atmosphere. The solids were washed with anhydrous methanol (3×10 ml) and the filtrate concentrated under reduced pressure. Anhydrous benzene (60 ml) was added to the residue, the mixture reconcentrated in vacuo and the residue was dried under high vacuum. Anhydrous dimethylformamide (10 ml), anhydrous tetrahydrofuran (20 ml) and methyl 4-methyl-2-phenyl-2H-1,2,3-triazole-5-carboxylate (1.00 g, 4.60 mmol) were added to the solid residue and the resulting mixture was heated at 70° C. under nitrogen for 7 h, then stirred at ambient temperature overnight. The reddish colored solution was then diluted with water (90 ml) to give the free base corresponding to the title compound as a tan solid (0.53 g, 47% yield).

Workup

  1. additionadded in one portion at room temperature
  2. filtrationfiltered under a nitrogen atmosphere
  3. washThe solids were washed with anhydrous methanol (3×10 ml)
  4. concentrationthe filtrate concentrated under reduced pressure
  5. additionAnhydrous benzene (60 ml) was added to the residue
  6. customthe residue was dried under high vacuum
  7. stirringstirred at ambient temperature overnight

Sources & evidence

ORD record
ord-a4696c1e38c44b4da380132238b94530
Source dataset
uspto-grants-2002_12
Patent number
US06492401B1

Reaction notes

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