HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496137Generated: October 30, 2026
2-Bromopyridine → HCID 178527162, compound
https://huagongshe.com/reaction/496137
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 178527161 | HCID 178527161 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 178527162 | HCID 178527162 | 58.2% |
Reaction Steps
A mixture of 5-chloro-3-cyclohexyl-8-(dihydroxyboryl)-1,2-dihydro-1,2,4-benzothiadiazine-1,1-dioxide (440 mg, 1.28 mmol), 2-bromopyridine (0.14 ml, 1.50 mmol), Pd(PPh3)2Cl2 (10 mg, 2 mol %) in 1,2-dimethoxyethane (30 ml) and Na2CO3 (2M, 3 ml, 6 mmol) were refluxed under N2 for 24 h. The solvents were removed under reduced pressure and the residue was treated with saturated NH4Cl (10 ml) and extracted with EtOAc (2×40 ml). The organic layer was washed with water (20 ml), dried (Na2SO4) and the solvent was removed under reduced pressure. The product was purified by flash chromatography on SiO2 using EtOAc:n-hexane (2:1, v/v) as eluent, yielding 280 mg (58%) of 5-chloro-3-cyclohexyl-8-(2-pyridyl)-1,2-dihydro-1,2,4-benzothiadiazine-1,1-dioxide as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06943159B1 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-e140a232d55d4e9193502402ef7df038 |
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| Source note | uspto-grants-2005_09 |
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