Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | s-Triazine, 2,4-dichloro-6-piperidino- | HCID 209165 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 5137221 | HCID 5137221 | 98% |
Reaction Steps
Ammonia was bubbled for 5 min in a solution of 2,4-dichloro-6-piperidin-1-yl-[1,3,5]triazine (500 mg, 2.15 mmol) in dry 1,4-dioxane (20 mL). The solution was heated at 70° C. for 16 h in a sealed tube. The reaction mixture was allowed to cool to room temperature, and partitioned between AcOEt and a solution of sat. NH4Cl. After separation, the organic layer was washed with water and brine, dried over anhydrous Na2SO4, filtered and concentrated to afford the title compound 221 (453 mg, 2.12 mmol, 98% yield). LRMS: [MH]+=214.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06897220B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-400bd7ff54cc4074b457323a131ed6f0 |
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| Source note | uspto-grants-2005_05 |
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