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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660894Generated: October 27, 2026

Hydrochloric Acid → 5-(2-Fluoro-4-iodophenylamino)-6,8-dimethylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dione

https://huagongshe.com/reaction/1660894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
ReactantSodium NitriteHCID 23668193—
Reactant5-(4-Amino-2-fluorophenylamino)-6,8-dimethylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dioneHCID 136080887—
CatalystIodineHCID 807—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product5-(2-Fluoro-4-iodophenylamino)-6,8-dimethylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dioneHCID 13592900851.6%

Reaction Steps

The title compound was synthesized from compound 9E (1.74 g, 5.5 mmol) which was first dissolved in a 1:1 mixture of acetic acid and water (10 mL) at 0° C. Concentrated HCl (1.2 mL) in water (2 mL) was slowly added and the mixture stirred for 20 minutes. Sodium nitrite (381 mg, 5.5 mmol, 1 eq) in water (800 μL) was added and the solution stirred for 20 minutes. Potassium iodide (4.58 g, 27.6 mmol, 5 eq) and iodine (20 mg, cat) was added and the reaction allowed to RT then stirred for 1 hour at 90° C. After cooling, the mixture was evaporated in vacuo. The residue was purified by silica chromatography eluting with 10% methanol in DCM to give 1.21 g of the title compound (51%). [M+H] calc'd for C15H12FIN4O2, 427; found, 427.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030317B2
Source datasetuspto-grants-2011_10
ORD IDord-f9ec4e6b544c467bb3e3b756d0773e9f
Source noteuspto-grants-2011_10