Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 23033170 | HCID 23033170 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 12965738 | HCID 12965738 | — |
Reaction Steps
A 2.59 g portion of 4,6-dichloro-N-(4-fluorophenyl)-1,3,5-triazine was dissolved in 20 ml of acetonitrile, and 2.09 ml of diisopropylethylamine and 1.18 g of p-toluidine were added thereto and stirred overnight at room temperature. The reaction solution was mixed with water and extracted with ethyl acetate, and the organic layer was washed with 1 M hydrochloric 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 (1:9), and then the thus obtained crude product was crystallized from benzene, thereby obtaining 2.74 g of 6-chloro-N-(4-fluorophenyl)-N′-(4-methylphenyl)-1,3,5-triazine-2,4-diamine as a white solid.
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-317c2627e09342f5a4ff08eab52bf5a3 |
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| Source note | uspto-grants-2008_05 |
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