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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantTert-butyl (3-amino-2,6-dichloropyridin-4-yl)carbamateHCID 86724467—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 2,6-dichloro-3-(methylamino)pyridin-4-ylcarbamateHCID 117843103—

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376441B2
Source datasetuspto-grants-2016_06
ORD IDord-ffea92ef7a3a4e759d2fd9777e5ebe9e
Source noteuspto-grants-2016_06