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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477612Generated: November 2, 2026

Tetrahydrofuran → 1-tert-Butyl 3-methyl 4-[5-(4-chlorobenzyl)-4-oxo-4,5-dihydro-1,3,5-triazin-2-yl]piperazine-1,3-dicarboxylate

https://huagongshe.com/reaction/1477612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium CarbonateHCID 10340—
Reactant1-tert-Butyl 3-methyl piperazine-1,3-dicarboxylateHCID 2756819—
ReactantHCID 117839620HCID 117839620—
SolventWaterHCID 962—
Product1-tert-Butyl 3-methyl 4-[5-(4-chlorobenzyl)-4-oxo-4,5-dihydro-1,3,5-triazin-2-yl]piperazine-1,3-dicarboxylateHCID 11783981143.1%

Reaction Steps

To tetrahydrofuran solution (2.3 mL) of 1-tert-butyl 3-methyl piperazine-1,3-dicarboxylate (43 mg, 0.17 mmol), sodium carbonate (37 mg, 0.35 mmol) and 4-chloro-1-(4-chlorobenzyl)-1,3,5-triazin-2(1H)-one (45 mg, 0.17 mmol) synthesized in Reference Synthesis Example 11 were added and the resultant solution was stirred at room temperature for 1 day. After completion of the reaction, water was added thereto and extraction with chloroform from the resultant mixture was performed three times. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure and ethyl acetate was added to the obtained residue. The obtained solid was collected by filtration and dried under reduced pressure to obtain the title compound (34 mg, yield 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-6dc87ce909464561a9176036227b3e44
Source noteuspto-grants-2016_08