Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | HCID 67047753 | HCID 67047753 | — |
| Reactant | HCID 178418311 | HCID 178418311 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178517386 | HCID 178517386 | 62.1% |
Reaction Steps
A mixture of ethyl 3-cycloheptyl-3-oxo-2-(2,4,6-trifluorophenyl)propanoate (342 mg, 1.0 mmol), 3-amino-1,2,4-triazole (84 mg, 1.0 mmol), and tributylamine (185 mg, 1.0 mmol) is stirred under nitrogen atmosphere at 160° C. for 2.5 h and cooled to room temperature. The mixture is dissolved in ethyl acetate and the organic layer is washed with 1.0 N hydrochloric acid and saturated sodium chloride, dried over magnesium sulfate, and concentrated to a solid. The solid thus obtained is washed with hexanes to give crude 7-cycloheptyl-6-(2,4,6-trifluorophenyl)[1,2,4]triazolo[1,5-a]pyrimidin-5-ol as a light tan solid (225 mg). MS: m/z 363.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07507739B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-5bec2205b16f45e0a6de23685051a431 |
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| Source note | uspto-grants-2009_03 |
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