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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59034Generated: October 30, 2026

Methyl iodide → Ethyl 4-(4-amino-3-fluorophenoxy)-2-aminopyridin-3-yl-methyl-carbamate

https://huagongshe.com/reaction/59034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 44184952HCID 44184952—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(4-amino-3-fluorophenoxy)-2-aminopyridin-3-yl-methyl-carbamateHCID 44184953—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 4-(4-amino-3-fluorophenoxy)-2-aminopyridin-3-yl-carbamate (6a) (480 mg, 1.6 mmol) was dissolved in dry THF (8 mL) and cooled at 0° C. Sodium hydride (60% in mineral oil, 80 mg, 2.0 mmol) was added, and the reaction mixture was stirred for 40 minutes at 0° C. Methyl iodide (130 μL, 1.8 mmol) was added at 0° C. The ice bath was removed, and the mixture was stirred at room temperature for 18 hours. The solvent was evaporated and the residue partitioned between DCM and distilled water. The organic layer was dried and evaporated, and the residue washed with diethyl ether to afford the title compound as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09439893B2
Source datasetuspto-grants-2016_09
ORD IDord-a6a7927ccafc42cbba750418631099e6
Source noteuspto-grants-2016_09