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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100516Generated: October 30, 2026

5-Phenyl-1-pentanol → HCID 135899209, compound

https://huagongshe.com/reaction/2100516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Phenyl-1-pentanolHCID 61523—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 136345786HCID 136345786—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 135899209HCID 13589920932%

Reaction Conditions

Temperature120 °C

Reaction Steps

2-Chloro-5-methyl-3H-pyrido[2,3-d]pyrimidin-4-one hydrochloride (36 mg, 155 μmol) was dissolved in DMSO (0.8 ml). Molecular sieves 4Å, 5-phenyl-1-pentanol (80 μl, 465 μmmol) and potassium tert-butylate (35 mg, 310 μmol) were added and the suspension was stirred at 120° C. for 48 h under an argon atmosphere. The molecular sieves were filtered off, the filtrate was poured onto ice water/isopropyl acetate 1/1, the layers were separated and the aqueous layer was extracted two times with isopropyl acetate. The combined extracts were washed with brine, dried over sodium sulfate and the solvent was removed under reduced pressure. The crude product was purified by column chromatography (silica gel, isopropyl acetate/heptane) to give 5-methyl-2-(5-phenyl-pentyloxy)-3H-pyrido[2,3-d]pyrimidin-4-one (16 mg, 50 μmol; 32%) as yellow crystals. MS: m/e=324.4 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572801B2
Source datasetuspto-grants-2009_08
ORD IDord-ba15645d65eb4049b3e0d587993f8161
Source noteuspto-grants-2009_08