Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1794093Erstellt: 27. Oktober 2026

2,4-Dimethylbenzyl alcohol → 2,4-Dimethylbenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochloride

https://huagongshe.com/reaction/1794093

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4-Dimethylbenzyl alcoholHCID 27809—
Eduktrel-1,1-Dimethylethyl (3R,5S)-4-(chlorocarbonyl)-3,5-dimethyl-1-piperazinecarboxylateHCID 86585999—
Produkt2,4-Dimethylbenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochlorideHCID 69142613—

Reaktionsschritte

2,4-Dimethylbenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochloride was prepared from cis 1-chlorocarbonyl-2,6-dimethyl-4-tert-butoxycarbonylpiperazine and 2,4-dimethylbenzyl alcohol according to the methods described for Examples 52 and 54 to give the product as a hygroscopic white solid (0.1384 g, 44% overall); (Found: C, 60.9; H, 8.1; N, 8.9%. C16H24N2O2.HCl.0.25H2O requires C, 60.6; H, 8.1; N, 8.8%); δH (400 MHz, DMSO-d6) 9.53 (2H, br), 7.19 (1H, d, J 7.6 Hz), 7.03 (1H, s), 6.99 (1H, d, J 7.6 Hz), 5.07 (2H, s), 4.29 (2H, m), 3.13 (2H, d, J 13.2 Hz), 3.04 (2H, dd, J 5.2 and 13.2 Hz), 2.27 (3H, s), 2.26 (3H, s) and 1.29 (6H, d, J 7.2 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07022707B2
Quelldatensatzuspto-grants-2006_04
ORD IDord-8a88cba5c0554d5db10ce66dd8c3f4a8
Quellennotizuspto-grants-2006_04