HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223824Generated: November 4, 2026
Water → N,N'-diphenyl-N''-(4-pyridylmethyl)-1,3,5-triazine-2,4,6-triamine
https://huagongshe.com/reaction/2223824
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,3,5-Triazine-2,4-diamine, 6-chloro-N2,N4-diphenyl- | HCID 16088 | — |
| Reactant | 4-Pyridinemethanamine | HCID 77317 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N,N'-diphenyl-N''-(4-pyridylmethyl)-1,3,5-triazine-2,4,6-triamine | HCID 10150345 | — |
Reaction Steps
A 200 mg portion of 6-chloro-N,N′-diphenyl-1,3,5-triazine-2,4-diamine was dissolved in 10.0 ml of acetonitrile, and 145 mg of 4-(aminomethyl)pyridine and 0.585 ml of diisopropylethylamine were added thereto and stirred overnight at 80° C. The reaction solution was cooled down to room temperature, and then mixed with water and extracted with chloroform. The organic layer was washed with 5% citric acid and saturated brine and then dried using anhydrous magnesium sulfate. The solvent was evaporated under a reduced pressure, the thus obtained residue was applied to a silica gel column chromatography and eluted with ethyl acetate:n-hexane (2:1), and then the thus obtained crude product was crystallized from ethyl acetate/n-hexane, thereby obtaining 107 mg of N,N′-diphenyl-N″-(4-pyridylmethyl)-1,3,5-triazine-2,4,6-triamine as light red crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07375222B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-0567f529f8734978bf303f29f1f859c5 |
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| Source note | uspto-grants-2008_05 |
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