HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365303Generated: October 31, 2026
Thionyl Chloride → HCID 23291098, compound
https://huagongshe.com/reaction/365303
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | 2-(Quinolin-2-YL)acetic acid | HCID 4711784 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 23291098 | HCID 23291098 | — |
Reaction Steps
Thionyl chloride (6 ml) was added to a suspension of quinaldinic acid (3.463 g, 20 mmol) in chloroform (40 ml). After the resulting mixture was heated under reflux and stirring for 6 hours, the solvent was distilled off. The residue was dissolved in acetone (50 ml), followed by the addition of a solution of N-benzylpiperazine (10.576 g, 60 mmol) in acetone (50 ml). The thus-obtained mixture was stirred for 1 hour. A deposited precipitate was removed, and the solvent was distilled off. The residue was dissolved in ethyl ether. The resulting solution was washed with an aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was dissolved in methanol, followed by the addition of concentrated hydrochloric acid (5 ml) for acidification. The solvent was distilled off and the thus-obtained residue was crystallized from a mixed solvent of ethanol and methanol, whereby 7.166 g of the title compound were obtained as white powder (yield: 97.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06127360 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-0debfc1f785f4189a107bae53f0f3f30 |
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| Source note | uspto-grants-2000_10 |
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