HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052502Generated: November 1, 2026
1-Isopropylpiperazine → 1-(4-Isopropylpiperazin-1-yl)hex-5-yn-1-one
https://huagongshe.com/reaction/1052502
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Isopropylpiperazine | HCID 78013 | — |
| Reactant | 5-Hexynoic acid | HCID 143036 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Isopropylpiperazin-1-yl)hex-5-yn-1-one | HCID 66545534 | 38.4% |
Reaction Steps
1-Isopropylpiperazine (228 mg, 1.78 mmol) was added over a mixture of hex-5-ynoic acid (200 mg, 1.78 mmol), N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (393 mg, 2.05 mmol) and N,N-dimethylpyridin-4-amine (10 mg, 0.05 mmol) in dichloromethane (10 ml) at 0° C. and the resulting mixture was stirred at room temperature overnight. 100 ml of dichloromethane were added and washed with sodium bicarbonate 4%. Then a solution of hydrogen chloride 0.5 N was added to the organic phase. The aquose phase was separated and neutralised with a solution of NaOH 2N and treated with ethyl acetate. The ethyl acetate phase was washed with water and brine, dried over magnesium sulphate and the solvent removed to give 152 mg (34% yield) of the title compound. Purity 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388189B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-cb57b4774c8c4f5cb6b05ce7e4dbace0 |
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| Source note | uspto-grants-2016_07 |
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