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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399573Generated: October 27, 2026

Diisopropylethylamine → Methyl 2-(2-(2-chlorophenyl)-4-methyl-6-phenylpyrimidin-5-yl)pentanoate

https://huagongshe.com/reaction/1399573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chlorophenylboronic acidHCID 2734322—
ReactantMethyl 2-(2-chloro-4-methyl-6-phenylpyrimidin-5-yl)pentanoateHCID 86665646—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 2-(2-(2-chlorophenyl)-4-methyl-6-phenylpyrimidin-5-yl)pentanoateHCID 5099697166.1%

Reaction Steps

Methyl 2-(2-chloro-4-methyl-6-phenylpyrimidin-5-yl)pentanoate (100 mg; 0.314 mmol), 2-chlorophenylboronic acid (73.6 mg; 0.471 mmol) and tetrakis(triphenylphosphine) palladium(0) (36.2 mg; 0.031 mmol) were placed in a 5 mL reaction tube and dissolved in a mixture of degassed DME (1.50 mL) and water (0.5 mL). N,N-Diisopropylethylamine (0.193 mL; 1.255 mmol) was added, the tube was sealed and irradiated in a microwave oven at 130° C. for 1 h. The reaction mixture was partitioned between brine and ethyl acetate, the phases were separated and the water layer was extracted with ethyl acetate. The combined organic layers were 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 82 mg (66%) of the title compound. ESI/APCI(+): 395 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906906B2
Source datasetuspto-grants-2014_12
ORD IDord-7b473e1f32144782baccf61761d51cd0
Source noteuspto-grants-2014_12