HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209014Generated: October 29, 2026
Methyl iodide → Tert-butyl 2,6-dichloro-3-(methylamino)pyridin-4-ylcarbamate
https://huagongshe.com/reaction/2209014
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | Tert-butyl (3-amino-2,6-dichloropyridin-4-yl)carbamate | HCID 86724467 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Tert-butyl 2,6-dichloro-3-(methylamino)pyridin-4-ylcarbamate | HCID 117843103 | — |
Reaction Steps
Palladium (II) acetate (0.21 g, 0.31 mmol) and 2-Dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (X-phos) (0.36 g, 0.75 mmol) were combined in toluene and heated at 120° C. for 3 min in microwave reactor. To this mixture tert-butyl 3-amino-2,6-dichloropyridin-4-ylcarbamate 2.43 (0.87 g, 3.12 mmol), Cs2CO3 (3.06 g, 9.38 mmol) and methyl iodide (0.196 mL, 3.12 mmol) were added and heated at 90° C. for 2 hr in a microwave reactor. After completion of the reaction, solvent was removed under reduced pressure. Solids were dissolved and extracted with ethyl acetate and water. Organic layer was washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. The residue obtained was heated in acetonitrile and solids were filtered out to obtain tert-butyl 2,6-dichloro-3-(methylamino)pyridin-4-ylcarbamate 2.44 that was used for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376441B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-ffea92ef7a3a4e759d2fd9777e5ebe9e |
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| Source note | uspto-grants-2016_06 |
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