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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300076Generated: November 1, 2026

Sodium hydride → 8-(3-Phenoxypropyl)-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-one

https://huagongshe.com/reaction/2300076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBenzene, (3-bromopropoxy)-HCID 68522—
Reactant2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 10514073—
SolventDimethylformamideHCID 6228—
Product8-(3-Phenoxypropyl)-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 18374769—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of NaH (51 mg of a 60% suspension of NaH in mineral oil) in 6 mL of dimethylformamide was added 2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-one (200 mg, 0.84 mmol). The reaction mixture was heated to 50° C. resulting in a yellow solution. The solution was cooled slightly, and 3-phenoxypropyl bromide (230 μL, 1.47 mmol) was added. The reaction mixture was heated at 50° C. for 10 minutes, then cooled to room temperature and partitioned between water and ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. Methanol and ethyl acetate were added to the residue, and 60 mg (19%) of 8-(3-phenoxypropyl)-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-one was collected by filtration, mp 175-176° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498163B1
Source datasetuspto-grants-2002_12
ORD IDord-8be5717a1dc0407381958bb89376b357
Source noteuspto-grants-2002_12