HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488795Generated: October 28, 2026
Guanidine Hydrochloride → HCID 178433869, compound
https://huagongshe.com/reaction/488795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl 5-methyl-2-phenyl-2H-1,2,3-triazole-4-carboxylate | HCID 2774347 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178433869 | HCID 178433869 | 47% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06974813B2 |
|---|
| Source dataset | uspto-grants-2005_12 |
|---|
| ORD ID | ord-681c085159074b1aa0c6834835ee9377 |
|---|
| Source note | uspto-grants-2005_12 |
|---|