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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167228Generated: November 1, 2026

Tetrahydrofuran → N-(2-acetamidophenyl)-3-fluoro-5-[(2-fluoro-4-iodophenyl)amino]isonicotinamide

https://huagongshe.com/reaction/2167228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHexamethyldisilazaneHCID 13838—
ReactantN-(2-aminophenyl)-3-fluoro-5-[(2-fluoro-4-iodophenyl)amino]isonicotinamideHCID 67513903—
ProductN-(2-acetamidophenyl)-3-fluoro-5-[(2-fluoro-4-iodophenyl)amino]isonicotinamideHCID 67514777—

Reaction Steps

69 mg of N-(2-aminophenyl)-3-fluoro-5-[(2-fluoro-4-iodophenyl)amino]isonicotinamide (0.148 mmol, 1 eq.) were dissolved in 1 mL of terahydrofurane under a nitrogen athmoshere, then 0.592 ml of a hexamethyl disilazane solution (1M in THF, 4 eq.) were added and stirring was continued at room temperature for 18 h. The reaction mixture was partitioned between 20 ml of ethyl acetate and 15 ml of aqueouse HCL solution (1M). The aqueouse layer was reextracted twice with 20 ml of ethyl acetate each. The combined organic layers were washed with 20 ml of brine, dried over a silicone filter and concentrated in vacuo. The residue was purified by flash chromatography to yield 14 mg (0.03 mmol, 19%) of the analytically pure target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045429B2
Source datasetuspto-grants-2015_06
ORD IDord-a820773abae44027a9b478bf8396776a
Source noteuspto-grants-2015_06