HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951656Generated: November 3, 2026
Sodium Carbonate → [6-Chloro-4-(2-chloro-phenyl)-pyridin-3-yl]-methyl-amine
https://huagongshe.com/reaction/1951656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Chlorophenylboronic acid | HCID 2734322 | — |
| Reactant | 6-chloro-4-iodo-N-methylpyridin-3-amine | HCID 57443400 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [6-Chloro-4-(2-chloro-phenyl)-pyridin-3-yl]-methyl-amine | HCID 23502811 | 83.9% |
Reaction Steps
A mixture of 6.05 g (19.3 mmol) (6-chloro-4-iodo-pyridin-3-yl)-methyl-amine, 23.6 g (23.6 mmol) 2-chlorophenylboronic acid, 441 mg (1.96 mmol) palladium(II) acetate, 1.03 g (3.93 mmol) triphenylphosphine, 47.1 ml 2 N sodium carbonate solution and 50 ml 1,2-dimethoxyethane was heated at 80° C. for 90 min. The reaction mixture was cooled to room temperature and diluted with 100 ml ethyl acetate. The aqueous layer was separated and extracted with 100 ml ethyl acetate. The combined organic layers were dried over sodium sulfate, concentrated in vacuo and purified by flash chromatography to give 4.1 g (83%) of the title compound as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404708B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-36d48408eac64ffb9489da1f959482b5 |
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| Source note | uspto-grants-2013_03 |
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