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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752112Generated: October 29, 2026

Sodium Hydroxide → HCID 57377802, compound

https://huagongshe.com/reaction/1752112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant6-chloro-2-N,4-N-dipropyl-1,3,5-triazine-2,4-diamineHCID 18304—
ReactantO-Allylhydroxylamine hydrochlorideHCID 3084724—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57377802HCID 5737780288.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2-chloro-N-(4,6-bis-(n-propylamino)-[1,3,5]triazine (XXXIV) (2.00 g, 8.71 mmol), O-allyl-hydroxylamine hydrochloride (1.91 g, 17.42 mmol) and NaOH (0.70 g, 17.42 mmol) in 1,4-dioxane (25 mL) and water (5 mL) was heated at 60° C. for 4 h. The volatiles were removed under reduced pressure. Saturated NaHCO3 solution (100 mL) was added to the residue and the mixture was extracted with EtOAc (3×25 mL). The combined organic extracts were washed with water (50 mL), brine (50 mL) and dried over Na2SO4. The solvent was removed under reduced pressure and the crude product was purified by flash column chromatography using gradient elution from CH2Cl2/EtOH (99:1) to CH2Cl2/EtOH (95:5) to yield O-allyl-N-(4,6-bis-propylamino-[1,3,5]triazin-2-yl)-hydroxylamine (XLIII, 2.05 g, 88% yield). ESI-MS (m/z) 267 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162992B2
Source datasetuspto-grants-2015_10
ORD IDord-941fd463680548e5afe95ee827431e76
Source noteuspto-grants-2015_10