HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094791Generated: October 31, 2026
Potassium Carbonate → 3-(2,3-Dichlorophenyl)pyridine-2,6-diamine
https://huagongshe.com/reaction/1094791
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromopyridine-2,6-diamine | HCID 1415868 | — |
| Reactant | 2,3-Dichlorobenzeneboronic acid | HCID 2734661 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(2,3-Dichlorophenyl)pyridine-2,6-diamine | HCID 57582357 | 35.4% |
Reaction Steps
To a suspension of 3-bromopyridine-2,6-diamine (0.376 g, 2.00 mmol) in 1,4-dioxane (12 ml) and water (6 ml) was added 2,3-dichlorophenyl boronic acid (0.573 g, 3.00 mmol), potassium carbonate (0.552 g, 4.00 mmol) and palladium tetrakis(triphenylphosphine) (0.115 g, 0.01 mmol). The reaction was purged with nitrogen and heated at 80° C. for 18 hours. Further palladium tetrakis(triphenylphosphine) (0.115 g, 0.01 mmol) and 2,3-dichlorophenyl boronic acid (0.573 g, 3.00 mmol) were added and the reaction heated at 80° C. for a further 18 hours before concentrating in vacuo. The residue was taken up in ethyl acetate (20 ml) and washed with a saturated aqueous solution of K2CO3 before drying over MgSO4 and concentrating in vacuo. The residue was purified by silica gel column chromatography, eluting with 99:1 dichloromethane:methanol, then recrystallised from toluene to afford the title compound (0.180 g, 35% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08134007B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-5942b936a5a347159b26a14ee07cd957 |
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| Source note | uspto-grants-2012_03 |
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