HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410385Generated: October 25, 2026
Sodium Acetate → 4-[5-Benzyl-3-(4-chloro-phenyl)-[1,2,4]triazol-1-yl]-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine
https://huagongshe.com/reaction/1410385
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-Hydrazinyl-6-(pyridin-2-yl)-1,3,5-triazin-2-amine | HCID 608952 | — |
| Reactant | N-(4-chloro-thiobenzoyl)-2-phenyl-acetamide | HCID 22174859 | — |
| Reactant | HOAc dioxane | HCID 22565020 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[5-Benzyl-3-(4-chloro-phenyl)-[1,2,4]triazol-1-yl]-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine | HCID 22174868 | 60% |
Reaction Steps
To a solution of N-(4-chloro-thiobenzoyl)-2-phenyl-acetamide (0.536 g, 1.85 mmol) and sodium acetate (ca. 0.25 g) in 1:1 acetic acid/1,4-dioxane (30 mL) was added 4-hydrazino-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine (0.376 g, 1.85 mmol). The solution was heated to 90° C. and stirred for 15 hours. The reaction mixture was allowed to cool to room temperature, and water (100 mL) was added. The precipitate was removed by filtration, triturated with hot ethanol (300 mL), and dried to provide 0.489 g (60%) of the product as a white solid: 1H NMR (DMSO-d6) δ 8.78 (d, J=4.3 Hz, 1H), 8.32 (d, J=6.1 Hz, 2H), 8.22 (d, J=7.8 Hz, 1H), 8.06 (d, J=8.5 Hz, 2H), 7.96 (dt, J=1.5, 7.8 Hz, 1H), 7.62-7.57 (m, 3H), 7.36-7.26 (m, 2H), 7.24-7.22 (m, 2H), 7.19-7.16 (m, 1H), 4.90 (s, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921547B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-78e2d5eb3c164f889f1ed70b47f636d2 |
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| Source note | uspto-grants-2014_12 |
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