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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-Ethyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine | HCID 21912722 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Bromo-2-ethyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine | HCID 21912794 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06511994B2 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-9f9e7f9a3012464680401c9c83aa8492 |
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| Source note | uspto-grants-2003_01 |
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