HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407180Generated: October 30, 2026
Ammonium Chloride → HCID 58360364, compound
https://huagongshe.com/reaction/407180
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | Ethyl 1-formyl-4-oxo-4H-quinolizine-3-carboxylate | HCID 20634151 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58360364 | HCID 58360364 | — |
Reaction Steps
To a solution of 2,5-dibromopyridine (2.00 g, 8.44 mmol) in 50 mL of toluene at −78° C. was added n-butyllithium (2.5 M in toluene, 4.05 mL, 10.1 mmol) dropwise. After 2 h, a solution of ethyl 1-formyl-4-oxo-4H-quinolizine-3-carboxylate (1.86 g, 7.60 mmoL) in 50 mL of dichloromethane was added dropwise. The mixture was warmed to rt, and after 1 h, treated with saturated aqueous ammonium chloride and concentrated in vacuo. The residue was redissolved in dichloromethane, washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified via silica gel chromatography, eluting with 30-100% ethyl acetate in hexanes to provide ethyl 1-[(5-bromopyridin-2-yl)(hydroxyl)methyl]-4-oxo-4H-quinolizine-3-carboxylate that gave a mass ion (ES+) of 404.7 (81Br) for [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754220B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-892b29df34474d92aa0c3e7d6a238bcd |
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| Source note | uspto-grants-2014_06 |
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