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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399593Generated: October 30, 2026

1-Iodopropane → HCID 66955906, compound

https://huagongshe.com/reaction/1399593

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodopropaneHCID 33643—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 66955978HCID 66955978—
SolventDimethylformamideHCID 6228—
ProductHCID 66955906HCID 6695590674%

Reaction Conditions

Temperature-15 °C

Reaction Steps

A solution of methyl 2-(4-(3-(methoxymethoxy)phenyl)-6-methyl-2-phenylpyrimidin-5-yl)acetate (79 mg; 0.209 mmol) in dry DMF (1 mL) was cooled to −15° C. (acetone/ice). LHMDS (0.230 mL; 0.230 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 (0.031 mL; 0.313 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, 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 (2-10%) in heptane to give 65 mg (73%) of the title compound as a colorless oil. ESI/APCI(+): 421 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906906B2
Source datasetuspto-grants-2014_12
ORD IDord-224c9d3a0a964f209967d9584c5e6e61
Source noteuspto-grants-2014_12