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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752107Generated: November 2, 2026

Methanamine, N-methoxy-, hydrochloride (1:1) → N2-Methoxy-N2-methyl-N4-propyl-1,3,5-triazine-2,4,6-triamine

https://huagongshe.com/reaction/1752107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-4-chloro-6-propylamino-s-triazineHCID 539913—
SolventEthanolHCID 702—
ProductN2-Methoxy-N2-methyl-N4-propyl-1,3,5-triazine-2,4,6-triamineHCID 5737780489%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 6-amino-2-chloro-4-n-propylamino-[1,3,5]triazine (XXXVIII) (5 g, 26.65 mmol), N,O-dimethylhydroxylamine hydrochloride (13 g, 133.24 mmol) and DIPEA (27.5 g, 213.2 mmol) in EtOH (100 mL) was heated at 100° C. for 16 h, after which time the solvent was removed under reduced pressure. The residue was dissolved in EtOAc (400 mL), which was washed with water (200 mL) and then with a brine solution (200 mL) and finally dried over Na2SO4. The solvent was removed under reduced pressure to yield N-(6-amino-4-n-propylamino-[1,3,5]triazin-2-yl)-N,O-dimethyl-hydroxylamine (XXXIX) as a white solid (5 g, 89% yield). LCMS (ESI) m/z=213 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162992B2
Source datasetuspto-grants-2015_10
ORD IDord-beecc9ef2f1a4e47b04e3718f4bea178
Source noteuspto-grants-2015_10