HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485029Generated: October 31, 2026
tert-Butanol → 1-Methyl-5-phenoxy-1H-pyrazol-4-ylamine
https://huagongshe.com/reaction/1485029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 84016145 | HCID 84016145 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-Methyl-5-phenoxy-1H-pyrazol-4-ylamine | HCID 86718551 | — |
Reaction Steps
To a stirred mixture of 1-Methyl-5-phenoxy-1H-pyrazole-4-carboxylic acid (16.00 g; 73.32 mmol), t-BuOH (51.20 g; 690.77 mmol) in 1,4-dioxane under argon was added DIPEA (37.44 g; 289.69 mmol) and Diphenylphosphoryl azide (41.60 g; 151.16 mmol). After 10 minutes at ambient temperature it was heated up to 110° C. and stirred there for 3 hours. The solvent was evaporated and the crude material purified by column chromatography. This compound was dissolved in DCM and treated with 4 M HCl in 1,4-dioxane. It was stirred for 2 days at ambient temperature. The solvent was evaporated and the residue dissolved in water and washed with EtOAc. The aqueous layer was basified with NaHCO3 solution and extracted with EtOAc. The organic layer was dried and concentrated to dryness.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422290B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-6d06588e089b4ce29141096132a74d9d |
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| Source note | uspto-grants-2016_08 |
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