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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-chloro-2-N,4-N-dipropyl-1,3,5-triazine-2,4-diamine | HCID 18304 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,2-Oxazinane hydrochloride | HCID 13010712 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-[1,2]oxazinan-2-yl-N,N'-dipropyl-[1,3,5]triazine-2,4-diamine | HCID 57377908 | 89% |
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
| 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-05129805e29540849e1a872ada95a143 |
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| Source note | uspto-grants-2016_05 |
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