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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399586Generated: October 30, 2026

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

https://huagongshe.com/reaction/1399586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chlorophenylboronic acidHCID 2734322—
ReactantMethyl 2-(2-chloro-4-methyl-6-p-tolylpyrimidin-5-yl)pentanoateHCID 86665647—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 2-(2-(2-chlorophenyl)-4-methyl-6-p-tolylpyrimidin-5-yl)pentanoateHCID 5099679381.5%

Reaction Steps

Methyl 2-(2-chloro-4-methyl-6-p-tolylpyrimidin-5-yl)pentanoate (100 mg; 0.300 mmol), 2-chlorophenylboronic acid (141 mg; 0.901 mmol), tetrakis(triphenylphosphine) palladium(0) (34.7 mg; 0.030 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 (0.185 mL; 1.202 mmol) was added, the tube was sealed and irradiated in a microwave oven at 130° C. for 40 min. 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 100 mg (81%) of the title compound. ESI/APCI(+): 409 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906906B2
Source datasetuspto-grants-2014_12
ORD IDord-e8a4b9dbf38c4114a7c55ab0c7615bb9
Source noteuspto-grants-2014_12