HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745210Generated: October 30, 2026
Water → 4-(2-Pyrimidinyl)-1-piperazinebutanamine
https://huagongshe.com/reaction/745210
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Piperazinebutanenitrile, 4-(2-pyrimidinyl)- | HCID 398654 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(2-Pyrimidinyl)-1-piperazinebutanamine | HCID 12840705 | — |
Reaction Steps
To a cold mixture of lithium aluminum hydride (2.0 g; 5.26 mmol) and anhydrous ether (240 ml) kept at a temperature of -54° C., there was dropwise added a solution of 1-(3-cyanopropyl)-4-(2-pyrimidinyl)piperazine (8 g; 3.46 mmol) in anhydrous ether (80 ml), and the resultant mixture was kept at the same temperature as above for 1.5 hours, followed by dropwise addition of water (2 ml), a 15% aqueous potassium hydroxide solution (2 ml) and water (6 ml) in order. The reaction mixture was stirred at room temperature for 2 hours, subjected to filtration with celite and washed with chloroform. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel chromatography to give 1-(4-aminobutyl)-4-(2-pyrimidinyl)-piperazine. IR νmaxFilm (cm--1): 3100-3600, 1580, 1540.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04598078 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-cf9a51052bbd46ffb89ef7c1054e2f6a |
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| Source note | uspto-grants-1986_07 |
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