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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067752Generated: October 26, 2026

Sodium hydride → (S)-3-(2,3-Dihydroxypropyl)-5-(2-fluoro-4-iodophenylamino)-6,8-dimethylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dione

https://huagongshe.com/reaction/2067752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(R)-(+)-4-(Chloromethyl)-2,2-dimethyl-1,3-dioxolaneHCID 2734443—
Reactant5-(2-Fluoro-4-iodophenylamino)-6,8-dimethylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dioneHCID 135929008—
SolventDimethylformamideHCID 6228—
Product(S)-3-(2,3-Dihydroxypropyl)-5-(2-fluoro-4-iodophenylamino)-6,8-dimethylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dioneHCID 2496642625.1%

Reaction Steps

Sodium hydride (67 mg, 3.5 mmol, 5 eq) was stirred in anhydrous DMF (500 μL) for 10 minutes. 5-(2-fluoro-4-iodophenylamino)-6,8-dimethylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dione (300 mg, 0.70 mmol, 1 eq, Example 12) in anhydrous DMF (300 μL) was added and the mixture stirred for 10 minutes. (R)-4-(Chloromethyl)-2,2-dimethyl-1,3-dioxolane (180 μL, 1.32 mmol, 5 eq) was added and the mixture subjected to microwave irradiation at 135° C. for 1 hour. The solvent was removed in vacuo. The residue was taken up in H2O (1 mL) and THF (1 mL). 1N HCl (1 mL) was added and the solution stirred at RT for 1 hour. After evaporation in vacuo the residue was purified by HPLC to give 88 mg (25%) of the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.64 (s, 3 H) 2.11 (s, 3 H) 3.18 (d, J=5.31 Hz, 1 H) 3.32-3.42 (m, 1 H) 3.63-3.70 (m, 1 H) 3.70-3.82 (m, 1 H) 4.24-4.38 (m, 1 H) 4.78 (t, J=5.56 Hz, 1 H) 5.09 (d, J=5.56 Hz, 1 H) 6.62 (t, J=8.72 Hz, 1 H) 7.45 (dd, J=7.71, 2.15 Hz, 1 H) 7.66 (dd, J=10.61, 2.02 Hz, 1 H) 8.48 (s, 1 H) 10.16 (s, 1 H) [M+H] calc'd for C18H18FIN4O4, 501; found, 501.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293901B2
Source datasetuspto-grants-2012_10
ORD IDord-25c3a571eaa64a7dbc779b71a43de6ec
Source noteuspto-grants-2012_10