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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794091Generated: October 31, 2026

2,3-Difluorobenzyl Alcohol → 2,3-Difluorobenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochloride

https://huagongshe.com/reaction/1794091

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Difluorobenzyl AlcoholHCID 447153—
Reactantrel-1,1-Dimethylethyl (3R,5S)-4-(chlorocarbonyl)-3,5-dimethyl-1-piperazinecarboxylateHCID 86585999—
Product2,3-Difluorobenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochlorideHCID 69143740—

Reaction Steps

2,3-Difluorobenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochloride was prepared from cis 1-chlorocarbonyl-2,6-dimethyl-4-tert-butoxycarbonylpiperazine and 2,3-difluorobenzyl alcohol according to the methods described for Examples 52 and 54 to give the product as a white solid (0.1846 g, 57% overall); (Found: C, 52.4; H, 6.0; N, 8.6%. C14H18F2N2O2.HCl requires C, 52.4; H, 6.0; N, 8.7%); δH (400 MHz, DMSO-d6) 10.07 (1H, br), 9.33 (1H, br), 7.44 (1H, m), 7.28 (2H, m), 5.21 (2H, s), 4.30 (2H, m), 3.14 (2H, d, J 13.2 Hz), 3.06 (2H, m), and 1.31 (6 H, d, J 7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022707B2
Source datasetuspto-grants-2006_04
ORD IDord-fd8e745e558e4f29855ab0d4871525db
Source noteuspto-grants-2006_04