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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635960Generated: October 31, 2026

Bromine → 3-Bromo-2-ethyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1635960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant2-Ethyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridineHCID 21912722—
SolventEthanolHCID 702—
Product3-Bromo-2-ethyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridineHCID 21912794—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-ethyl-4,5,6,7-tetrahydropyrazolo[1,5-α]pyridine (4.12 g, from Step 2) in EtOH (25 mL) was added Br2 (1.42 mL) dropwise at 0° C. The reaction was stirred at 0° C. for 20 min. The reaction mixture was partitioned between EtOAc and aqueous NaHCO3 (saturated). Aqueous layer was extracted with EtOAc (3×). Combined organic phase was washed with brine and dried over anhydrous MgSO4. After concentration, the residue was purified by flash chromatography with 10% EtOAc in hexanes followed by 20% EtOAc in hexanes to give the title compound as a viscous oil. 1H NMR (500 MHz, CDCl3) δ 1.25 (t, 3H, J=7.5 Hz), 1.80-1.90 (m, 2H), 1.95-2.05 (m, 2H), 2.55-2.70 (m, 4H), 4.07 (t, 2H, J=6.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06511994B2
Source datasetuspto-grants-2003_01
ORD IDord-9f9e7f9a3012464680401c9c83aa8492
Source noteuspto-grants-2003_01