HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238385Generated: October 29, 2026
1-Phenylpiperazine → HCID 86684883, compound
https://huagongshe.com/reaction/238385
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86684882 | HCID 86684882 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86684883 | HCID 86684883 | 103.4% |
Reaction Steps
A mixture of 1-phenylpiperazine (3.40 g), 5-[(4-chlorobenzyl)oxy]-1-methyl-1H-pyrazol-4-carbaldehyde (600 mg), triethylamine (1.20 mL) and dimethylformamide (7.0 mL) was stirred at 120° C. for 8 hours, and then at a room temperature for 17 hours. Thereafter, the reaction solution was concentrated under a reduced pressure, and water was then added thereto. The obtained mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated saline, and was then dried over anhydrous sodium sulfate, followed by vacuum concentration. The residue was purified by column chromatography (silica gel cartridge, hexane:ethyl acetate=80:20 to 10:90), so as to obtain the title compound (669 mg) in the form of a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642626B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-87197779fa3a49caabdcb9286e3c4e28 |
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| Source note | uspto-grants-2014_02 |
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