HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229321Generated: October 30, 2026
Water → 5-Bromo-n-(2,6-dichloro-4-methyl-3-pyridinyl)-2-(ethylamino)-3-pyridinecarboxamide
https://huagongshe.com/reaction/2229321
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | n-(2,6-Dichloro-4methyl-3-pyridinyl)-2-(ethylamino)-3-pyridinecarboxamide | HCID 10782273 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Bromo-n-(2,6-dichloro-4-methyl-3-pyridinyl)-2-(ethylamino)-3-pyridinecarboxamide | HCID 18466622 | — |
Reaction Steps
Solid KOAc (22.2 g, 229 mmol) was added to a solution of crude N-(2,6-dichloro-4methyl-3-pyridinyl)-2-(ethylamino)-3-pyridinecarboxamide (61.98 g, <190 mmol) in AcOH (600 mL). A solution of Br2 (9.7 mL, 191 mmol) was then added over 30 min. After stirring 30 min, additional amounts of KOAc and Br2 were introduced until TLC indicated that no starting material remained (a total of 11.2 g of KOAc and 5.91 mL of Br2). The solution was then poured into water (2 L) and stirred for 20 min. The solid was removed by filtration and then dissolved in Et2O (1 L). The ethereal solution was washed with water (3×), aqueous saturated NaHCO3, brine then dried (MgSO4) to give a mixture containing, as the major component, the title compound (77.7 g, yellow foam). The material was used directly in the subsequent reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06420359B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-b47e618e7ca24f2ab1cdcf597df120fe |
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| Source note | uspto-grants-2002_07 |
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