HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786115Generated: October 31, 2026
Dimethylamine → 4-(3-Buten-1-yl)-6-(dimethylamino)-2-hydrazino-1,3,5-triazine
https://huagongshe.com/reaction/1786115
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178418797 | HCID 178418797 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(3-Buten-1-yl)-6-(dimethylamino)-2-hydrazino-1,3,5-triazine | HCID 68848123 | — |
Reaction Steps
To a cyanuric chloride (1.07 g, 5.80 mmol) in anhydrous benzene (10.7 mL) was added at 0° C. dropwise a solution of 3-butenylmagnesium bromide (0.5M in THF, 12.8 mL, 6.38 mmol). The resulting mixture was stirred at 0° C. for 3 hrs. To the mixture were added 1,4-dioxane (10 mL), DIPEA (1.1 mL), followed by addition of dimethylamine (2.0M in MeOH, 3.2 mL, 6.38 mmol) at 0° C. The mixture was stirred and allowed to warm up to room temperature over 2 hours. Finally to it was added hydrazine hydrate (7.0 mL) at room temperature. The mixture was stirred at room temperature overnight. Then the volatiles were evaporated in vacuo. The residue was purified by HPLC to provide the title compound as a white solid. MH+209.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07507726B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-df1d91d0ebde4ebe867f1af20cecb905 |
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| Source note | uspto-grants-2009_03 |
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