HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381973Generated: October 28, 2026
Oxalic Acid → N-(6-Methyl-3-oxo-2,5-dihydro-1,2,4-triazin-4(3H)-yl)acetamide
https://huagongshe.com/reaction/2381973
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 5-Methyl-3-(2-oxopropyl)-1,3,4-oxadiazol-2(3H)-one | HCID 11040920 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | N-(6-Methyl-3-oxo-2,5-dihydro-1,2,4-triazin-4(3H)-yl)acetamide | HCID 11008343 | 70% |
Reaction Steps
To a solution of 5-methyl-3-(2-oxo-propyl)-3H-1,3,4-oxadiazol-2-one (2.052 g, 13.14 mmol) in a mixture of 2-propanol (12 mL) and water (0.3 mL) is added hydrazine monohydrate (0.96 mL, 19.8 mmol). The mixture is stirred at rt under N2 for 15 h, and then heated to reflux for 7 h. A solution of oxalic acid (0.363 g, 4.032 mmol) in 2-propanol (6 mL) is added to the warm reaction solution. The resulting precipitate is removed by filtration through a coarse porosity sintered glass funnel, and the filtrate is concentrated in vacuo to approximately 10 mL in total volume. The concentrated solution is chilled to −12° C., and the resulting crystals are collected by filtration and dried to afford N-(6-methyl-3-oxo-2,5-dihydro-3H-1,2,4-triazin-4-yl)-acetamide (1.562 g, 70%). MS: 171 (M+H); 1H NMR (300 MHz, CDCl3) δ 8.10 (br s, 1H), 7.57 (br s, 1H), 4.20 (s, 2H), 2.04 (s, 3H), 1.95 (s, 3H); 1H NMR (300 MHz, DMSO-d6) δ 9.98 (s, 1), 9.74 (s, 1), 4.04 (s, 2), 1.84 (s, 6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258130B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-7d849263b67941308c6bf26d2e136d00 |
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| Source note | uspto-grants-2012_09 |
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