HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341461Generated: November 2, 2026
Potassium Carbonate → 6-{5-[3-(Cyclopropylmethylamino)-pyridin-2-yl]-[1,2,4]oxadiazol-3-yl}-N-methyl-N-phenyl-[1,3,5]triazine-2,4-diamine
https://huagongshe.com/reaction/341461
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Cyclopropanemethanamine | HCID 75646 | — |
| Reactant | 6-[5-(3-Fluoropyridin-2-yl)-[1,2,4]oxadiazol-3-yl]-N-methyl-N-phenyl-[1,3,5]triazine-2,4-diamine | HCID 56942572 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-{5-[3-(Cyclopropylmethylamino)-pyridin-2-yl]-[1,2,4]oxadiazol-3-yl}-N-methyl-N-phenyl-[1,3,5]triazine-2,4-diamine | HCID 66802567 | 44% |
Reaction Steps
6-[5-(3-Fluoropyridin-2-yl)-[1,2,4]oxadiazol-3-yl]-N-methyl-N-phenyl-[1,3,5]triazine-2,4-diamine (prepared in an analogous manner to Example 482, 50 mg, 0.137 mmol), 1-cyclopropylmethanamine (24 μL, 0.274 mmol) and potassium carbonate (57 mg, 0.411 mmol) were suspended in anhydrous DMF (2 mL) in a sealed tube at room temperature under nitrogen. The reaction mixture was stirred at 90 C for 3 h and then at 100 C for 18 h. The mixture was diluted with DCM (10 mL) and then washed with saturated aq. ammonium chloride (3×5 mL) and then brine (5 mL). The organic layer was dried over sodium sulfate and evaporated under vacuum. The crude residue was purified by flash chromatography (0-1% (7M ammonia in MeOH) in DCM) to afford the title compound (25 mg, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895733B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-c1ecd5cfb6494ebdad5a0f952cfbae33 |
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| Source note | uspto-grants-2014_11 |
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