HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12873Generated: October 26, 2026
tert-Butylhydrazine monohydrochloride → 1-tert-butyl-5-(5-methyl-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid methyl ester
https://huagongshe.com/reaction/12873
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-Dimethylamino-2-(5-methyl-isoxazole-3-carbonyl)-acrylic acid ethyl ester | HCID 67020947 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-tert-butyl-5-(5-methyl-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid methyl ester | HCID 67021103 | 101.7% |
Reaction Steps
A solution of 3-dimethylamino-2-(5-methyl-isoxazole-3-carbonyl)-acrylic acid ethyl ester (27.53 mmol) in absolute ethanol (41.7 mL) was treated with tert-butylhydrazine hydrochloride (3.57 g, 28.63 mmol) and sodium acetate (2.80 g, 34.13 mmol). The resulting mixture was heated to 90° C. for 18 h. At this time, the reaction was cooled to 25° C. The reaction was diluted with water (200 mL) and was then extracted with dichloromethane (3×150 mL). The combined organics were dried over sodium sulfate, filtered and concentrated in vacuo to afford 1-tert-butyl-5-(5-methyl-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid methyl ester (7.37 g, 96%) as a black solid. The material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728029B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-992fdccc9f344eb986ca721d7e723ab4 |
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| Source note | uspto-grants-2010_06 |
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