HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1783987Erstellt: 25. Oktober 2026
4-Iodoaniline → Tert-butyl 4-(4-aminophenyl)-3-oxopiperazine-1-carboxylate
https://huagongshe.com/reaction/1783987
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Iodoaniline | HCID 10893 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Tert-butyl 3-oxopiperazine-1-carboxylate | HCID 3157178 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | Tert-butyl 4-(4-aminophenyl)-3-oxopiperazine-1-carboxylate | HCID 57437534 | 87% |
Reaktionsschritte
A suspension of p-iodo-aniline (918 mg, 4.8 mmol), 3-oxo-piperazine-1-carboxylic acid tert-butyl ester (960 mg, 4.2 mmol) (1R,2R)-cyclohexane-1,2-diamine (0.05 mL, 0.42 mmol), copper (I) iodide (14.9 mg, 0.0042 mmol) and K2CO3 (1.19 g, 2.04 mmol) in dioxane (4 mL), is purged with nitrogen for 5 min in a reaction tube. The tube is sealed and the reaction mixture is heated at 119° C. for 15 hours. After cooling to room temperature, the reaction mixture is filtered through a silica cartridge washing with ethyl acetate (40 mL). The filtrate is concentrated in vacuo to afford the title compound as a brown liquid (1.06 g, 87%). LCMS: Rt 0.88 min (91%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07501411B2 |
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| Quelldatensatz | uspto-grants-2009_03 |
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| ORD ID | ord-d3d356812b1f43bf9733b56ece81d4c4 |
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| Quellennotiz | uspto-grants-2009_03 |
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