HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530044Generated: October 30, 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/530044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Amino-4-chloro-6-propylamino-s-triazine | HCID 539913 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N2-Methoxy-N2-methyl-N4-propyl-1,3,5-triazine-2,4,6-triamine | HCID 57377804 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09351972B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-4e376dc0abc242408572130d018d7335 |
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| Source note | uspto-grants-2016_05 |
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