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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399578Generated: November 3, 2026

1-Iodopropane → Methyl 2-(4-methyl-2,6-diphenylpyrimidin-5-yl)pentanoate

https://huagongshe.com/reaction/1399578

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodopropaneHCID 33643—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantMethyl 2-(4-methyl-2,6-diphenylpyrimidin-5-yl)acetateHCID 66955384—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(4-methyl-2,6-diphenylpyrimidin-5-yl)pentanoateHCID 5099644255.4%

Reaction Conditions

Temperature-15 °C

Reaction Steps

A solution of methyl 2-(4-methyl-2,6-diphenylpyrimidin-5-yl)acetate (150 mg; 0.471 mmol) in dry DMF (2.5 mL) was cooled to −15° C. LHMDS (0.518 mL; 0.518 mmol; 1M in THF) was added dropwise and the mixture was stirred at −15° C. for 15 min followed by the dropwise addition of iodopropane (0.069 mL; 0.707 mmol), after stirring for 2 h at −15° C. the mixture was allowed to warm to room temperature. After 1 h the reaction was quenched by adding a saturated solution of ammonium chloride. The mixture was extracted twice with ethyl acetate and the combined organic layers were washed with brine and dried over magnesium sulphate and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica gel using a linear gradient of ethylacetate (1-10%) in heptane to give 94 mg (54%) of the title compound as a colorless oil. ESI/APCI(+): 361 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906906B2
Source datasetuspto-grants-2014_12
ORD IDord-6577dffaa6604e5fa795b1f14b3b9ce6
Source noteuspto-grants-2014_12