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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butylhydrazine monohydrochlorideHCID 81889—
Reactant3-Oxo-3-(pyridin-2-yl)propanenitrileHCID 11571823—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product2-tert-Butyl-5-pyridin-2-yl-2H-pyrazol-3-ylamineHCID 6729991862.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470820B2
Source datasetuspto-grants-2013_06
ORD IDord-acda246a8d9440a295ec7f6d081b381e
Source noteuspto-grants-2013_06