HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566113Generated: October 26, 2026
Triethylamine → N-(4-nitrobenzyl)-N-(2-pyrimidinyl)amine
https://huagongshe.com/reaction/566113
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzylamine | HCID 29147 | — |
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(4-nitrobenzyl)-N-(2-pyrimidinyl)amine | HCID 22569285 | 11% |
Reaction Steps
A mixture of 4-nitrobenzylamine (6.09 g, 40.0 mmol), 2-chloropyrimidine (4.82 g, 42.1 mmol), triethylamine (11.2 ml, 80.4 mmol) and ethanol (120 ml) was stirred at 110° C. for 24 hours, and the mixture was concentrated under reduced pressure. To the residue was added water, and the mixture was extracted with ethyl acetate-THF. The organic layer was dried with anhydrous sodium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-ethanol to give N-(4-nitrobenzyl)-N-(2-pyrimidinyl)amine (0.99 g, 4.3 mmol, 11%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06172061B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-7dba33416d7f4f3387a0bad7417f92c2 |
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| Source note | uspto-grants-2001_01 |
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