HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260317Generated: November 3, 2026
Triethylamine → 2-tert-Butyl-5-pyridin-2-yl-2H-pyrazol-3-ylamine
https://huagongshe.com/reaction/1260317
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Reactant | 3-Oxo-3-(pyridin-2-yl)propanenitrile | HCID 11571823 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-tert-Butyl-5-pyridin-2-yl-2H-pyrazol-3-ylamine | HCID 67299918 | 62.7% |
Reaction Steps
To a stirred solution of 3-oxo-3-pyridin-2-yl-propionitrile (0.40 g, 2.7 mmol; CAS 54123-21-6) at r.t. in EtOH (10 ml) under an argon atmosphere were added triethylamine (1.1 ml, 8.2 mmol) and t-butylhydrazine hydrochloride (1.02 g, 8.2 mmol). The mixture was heated to reflux and stirring was continued for 2 hrs. The orange solution was cooled to r.t. The solids were filtered off. The filtrate was concentrated to leave an orange viscous oil which was taken up in EtOAc and washed with water. The aqueous layer was extracted with EtOAc and with CH2Cl2/MeOH 9:1. The combined organics were dried over MgSO4, filtered and concentrated. After silica gel chromatography using CH2Cl2/MeOH as gradient, the product was obtained as off-white solid (0.366 g, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470820B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-acda246a8d9440a295ec7f6d081b381e |
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| Source note | uspto-grants-2013_06 |
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