Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399566Generated: November 1, 2026

1-Iodopropane → HCID 66955592, compound

https://huagongshe.com/reaction/1399566

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodopropaneHCID 33643—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 66955908HCID 66955908—
SolventDimethylformamideHCID 6228—
ProductHCID 66955592HCID 6695559279%

Reaction Conditions

Temperature-15 °C

Reaction Steps

A solution of methyl 2-(2-(dimethylamino)-4-methyl-6-phenylpyrimidin-5-yl)acetate (750 mg; 2.63 mmol) in dry DMF (13 mL) was cooled to −15° C. LHMDS (2.89 mL, 2.89 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 (0.385 mL; 3.94 mmol), after stirring for 2 h at −15° C. the mixture was allowed to warm up 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 (2-20%) in heptane to give 680 mg (79%) of the title compound as a white solid. 1H NMR (CDCl3) δ 7.46-7.40 (5H, m); 3.82 (1H, dd, J=6.1, 8.2 Hz); 3.69 (3H, s); 3.19 (6H, s); 2.31 (3H, s); 2.08-1.96 (1H, m); 1.62-1.47 (1H, m); 1.02-0.92 (2H, m); 0.65 (3H, t, J=7.1 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906906B2
Source datasetuspto-grants-2014_12
ORD IDord-98e42b5535814c8f85c1921eccb00b9a
Source noteuspto-grants-2014_12