HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778198Generated: November 3, 2026
tert-Butanol → 1-Methyl-5-phenoxy-1H-pyrazol-4-ylamine
https://huagongshe.com/reaction/1778198
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 (16.0 g; 73.3 mmol), t-BuOH (51.2 g; 691 mmol) in 1,4-dioxane under argon are added DIPEA (37.4 g; 290 mmol) and diphenylphosphoryl azide (41.6 g; 151 mmol). After 10 minutes at ambient temperature it is heated up to 110° C. and stirred for 3 hours. The solvent is evaporated and the crude material purified by column chromatography. This compound is dissolved in DCM and treated with 4 M HCl in 1,4-dioxane. It is stirred for 2 days at ambient temperature. The solvent is evaporated and the residue dissolved in water and washed with EtOAc. The aqueous layer is basified with aqueous NaHCO3 solution and is extracted with EtOAc. The organic layer is dried and concentrated to dryness.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266891B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-d0e2c83485044ceca1b6bec44f2d81ab |
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| Source note | uspto-grants-2016_02 |
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