HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 79209Erstellt: 25. Oktober 2026
Triethylamine → tert-Butyl 4-(2-chloronicotinoyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/79209
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Edukt | 6-Chloronicotinoyl Chloride | HCID 2782165 | — |
| Edukt | Dichloromethane methanol | HCID 21226129 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | tert-Butyl 4-(2-chloronicotinoyl)piperazine-1-carboxylate | HCID 4321619 | 89% |
Reaktionsschritte
To a stirred ice-cooled solution of tert-butyl 1-piperazinecarboxylate (2.2 g, 12 mmol), triethylamine (3.2 mL, 23 mmol), and 4-dimethylaminopyridine (0.014 g, 0.11 mmol) in DCM (15 mL) was added 6-chloropyridine-3-carbonyl chloride (2.0 g, 11 mmol) in one portion. The resulting mixture was stirred at 0° C. and gradually warmed up to ambient temperature for 20 h. Upon workup, the mixture was subjected to combi-flash column chromatography (methanol/DCM) to give compound 351 (3.3 g, 89% yield) as a white solid. 1H NMR (400 MHz, CDCl3) δ ppm 8.46 (1 H, d, J=2.0 Hz), 7.74 (1 H, dd, J=8.2, 2.3 Hz), 7.42 (1 H, dd, J=8.2, 0.8 Hz), 3.20-4.02 (8 H, m), 1.48 (9 H, s). LCMS-ESI (POS), M/Z, M+1: Found 326.0.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841312B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-af2914b2e197410da17757f6a76e2c5a |
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| Quellennotiz | uspto-grants-2014_09 |
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