HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931544Generated: November 2, 2026
2,6-Lutidine → 5-Amino-N-(triethylsilyl)-1H-1,2,4-triazole-3-carboxamide
https://huagongshe.com/reaction/1931544
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Triethylsilyl trifluoromethanesulphonate | HCID 2733308 | — |
| Reactant | 3-amino-1H-1,2,4-triazole-5-carboxamide(SALTDATA: FREE) | HCID 18707494 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Amino-N-(triethylsilyl)-1H-1,2,4-triazole-3-carboxamide | HCID 59312593 | 26.5% |
Reaction Steps
A stirred mixture of 3-amino-1H-1,2,4-triazole-5-carboxamide (103 mg, 0.810 mol) in 1,2-dichloroethane (1.62 mL) treated at room temperature with 2,6-lutidine (283 μL, 2.43 mmol) and triethylsilyl trifluoromethanesulfonate (458 μL, 2.03 mmol). After 22 hours the reaction was heated at 50° C. and after 1.5 hours of heating the reaction was allowed to cool to room temperature. The reaction mixture was diluted with ethyl acetate (20 mL) and washed with water (25 mL), dried over magnesium sulfate, filtered, and evaporated to an oil which was flash chromatographed (silica gel, 0-10% ethyl acetate:hexane) to give the title compound as a white solid (130 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08188085B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-5fb4753ee4434cab8649ff79e66580bc |
|---|
| Source note | uspto-grants-2012_05 |
|---|