HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250565Generated: October 26, 2026
Piperidine → 2-Chloro-6-nitro-4-piperidinoquinazoline
https://huagongshe.com/reaction/1250565
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-Nitro-2,4(1H,3H)-quinazolinedione | HCID 816982 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-6-nitro-4-piperidinoquinazoline | HCID 18326509 | — |
Reaction Steps
To 367 mg (1.77 mmol) of 6-nitroquinazoline-2,4 (1H,3H)-dione was added 15.13 g (98.70 mmol) of phosphorus oxychloride to effect reaction in the same manner as in Example 10. Next, to the reaction mixture was added dropwise 301 mg (3.54 mmol) of piperidine under ice cooling, and the resulting mixture was stirred under ice cooling for 2 hours. Water was added to the reaction mixture, and crystals thus precipitated were filtered out to obtain 2-chloro-6-nitro-4-piperidinoquinazoline. The compound was dissolved in 1 ml of DMF, and after 1.52 g (26.65 mmol) of allylamine was added to the resulting solution, the resulting mixture was stirred at room temperature for 2.5 hours. Water was added to the reaction mixture, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by a silica gel column to give 213 mg (yield: 38.4%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06339089B2 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-8d9ae0c038e542ffa98a4345f542b98d |
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| Source note | uspto-grants-2002_01 |
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