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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-tert-Butyl 3-methyl piperazine-1,3-dicarboxylate | HCID 2756819 | — |
| Reactant | HCID 117839620 | HCID 117839620 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-tert-Butyl 3-methyl 4-[5-(4-chlorobenzyl)-4-oxo-4,5-dihydro-1,3,5-triazin-2-yl]piperazine-1,3-dicarboxylate | HCID 117839811 | 43.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403798B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-6dc87ce909464561a9176036227b3e44 |
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| Source note | uspto-grants-2016_08 |
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