Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diphenylphosphoryl azide | HCID 123414 | — |
| Reactant | 5-Nitro-1H-pyrazole-3-carboxylic acid | HCID 86222684 | — |
| Product | 937040-09-0 | HCID 135971896 | — |
Reaction Steps
To 10 g (63.66 mmol) of 5-nitro-1H-pyrazole-3-carboxylic acid are respectively added 39 ml of tert-butanol, 27.44 ml (127.3 mmol) of diphenylphosphorazidate and 17.7 ml (127.32 mmol) of triethylamine. The solution is refluxed for 8 h, then an aqueous solution saturated with potassium carbonate is added until reaching pH 8, and the product is extracted several times with ethyl acetate. The organic phases are combined, dried over magnesium sulfate, and concentrated. The residue obtained is triturated in methanol to give 4.38 g of tert-butyl 5-nitro-1H-pyrazol-3-ylcarbamate in the form of a yellow solid. The filtrate is concentrated and purified by chromatography on silica (cyclohexane/ethyl acetate eluent: 7:3) to yield an additional 1.49 g of tert-butyl 5-nitro-1H-pyrazol-3-ylcarbamate in the form of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889711B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-52f8fe2e15e2415694cb6554a8830328 |
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| Source note | uspto-grants-2014_11 |
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