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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantCyanuric chlorideHCID 7954—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178418797HCID 178418797—
SolventBenzeneHCID 241—
Solvent1,4-DioxaneHCID 31275—
Product4-(3-Buten-1-yl)-6-(dimethylamino)-2-hydrazino-1,3,5-triazineHCID 68848123—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507726B2
Source datasetuspto-grants-2009_03
ORD IDord-df1d91d0ebde4ebe867f1af20cecb905
Source noteuspto-grants-2009_03