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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530060Generated: October 27, 2026

6-chloro-2-N,4-N-dipropyl-1,3,5-triazine-2,4-diamine → 6-[1,2]oxazinan-2-yl-N,N'-dipropyl-[1,3,5]triazine-2,4-diamine

https://huagongshe.com/reaction/530060

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-chloro-2-N,4-N-dipropyl-1,3,5-triazine-2,4-diamineHCID 18304—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant1,2-Oxazinane hydrochlorideHCID 13010712—
SolventTetrahydrofuranHCID 8028—
Product6-[1,2]oxazinan-2-yl-N,N'-dipropyl-[1,3,5]triazine-2,4-diamineHCID 5737790889%

Reaction Conditions

Temperature100 °C

Reaction Steps

An ACE® pressure tube was charged with 2-chloro-N-(4,6-bis-(n-propylamino)-[1,3,5]triazine (XXXIV) (1.50 g, 6.53 mmol), N-ethyldiisopropylamine (19.59 mmol), 1,2-oxazinane hydrochloride (1.61 g, 13.06 mmol) and tetrahydrofuran. The reaction mixture was heated at 100° C. for 2 h, then cooled and poured into saturated NaHCO3 solution (50 mL). The suspension 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 6-[1,2]oxazinan-2-yl-N,N′-dipropyl-[1,3,5]triazine-2,4-diamine (LVII) (1.63 g, 89%). ESI-MS (m/z): 281 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09351972B2
Source datasetuspto-grants-2016_05
ORD IDord-05129805e29540849e1a872ada95a143
Source noteuspto-grants-2016_05