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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272678Generated: November 2, 2026

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

https://huagongshe.com/reaction/2272678

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 numberUS09120789B2
Source datasetuspto-grants-2015_09
ORD IDord-4c39f5d9f96943498afaf75ed55f763b
Source noteuspto-grants-2015_09