HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913049Generated: October 27, 2026
Dimethylformamide → 3,4-dicyclopropyl-5-(4-pentylbicyclo[2.2.2]oct-1-yl)-4H-1,2,4-triazole
https://huagongshe.com/reaction/913049
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl triflate | HCID 9526 | — |
| Reactant | Cyclopropanecarboxylic acid cyclopropylamide | HCID 351205 | — |
| Reactant | 4-Pentylbicyclo[2.2.2]octane-1-carbohydrazide | HCID 22591694 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3,4-dicyclopropyl-5-(4-pentylbicyclo[2.2.2]oct-1-yl)-4H-1,2,4-triazole | HCID 11174824 | — |
Reaction Steps
To a solution of N-cyclopropylcyclopropanecarboxamide (2-A) (26 mg, 0.210 mmol) in 0.50 ml toluene was added methyl triflate (1.45 mg, 1 eq) and the reaction was heated at 100° C. for 5-7 min until all of the amide went into solution. To this crude solution was added 0.740 mL of a 0.3 M solution of 4-pentylbicyclo[2.2.2]octane-1-carbohydrazide in DMF (1.1 eq, crude, prepared as described in Step A of Example 1) followed by triethylamine (0.059 mL, 2 eq) and the mixture was heated at 130° C. for 4 h. After this time the solvent was removed under reduced pressure, and the residue was chromatographed on C-18 reverse phase (gradient 90% water to 100% acetonitrile, 0.1% TPA). The fractions containing the compound were determined by LCMS, added to 200 mL of methylene chloride, and extracted with saturated aqueous sodium bicarbonate. The organic layer was dried over magnesium sulfate and evaporated under diminished. The residue was lyophilized from benzene to afford 3,4-dicyclopropyl-5-(4-pentylbicyclo[2.2.2]oct-1-yl)-4H-1,2,4-triazole (2-B); MS (ESI+)=328.3 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026264B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-ccf9927c7ff24b85a97bb67107f64af1 |
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| Source note | uspto-grants-2011_09 |
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