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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794108Generated: October 25, 2026

(R)-4-Difluoromethoxybenzyl 2-ethylpiperazine-1-carboxylate fumarate → (R)-2,6-Difluoro-4-difluoromethoxybenzyl 2-methylpiperazine-1-carboxylate fumarate

https://huagongshe.com/reaction/1794108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-4-Difluoromethoxybenzyl 2-ethylpiperazine-1-carboxylate fumarateHCID 21021913—
ReactantBenzenemethanol, 4-(difluoromethoxy)-2,6-difluoro-HCID 69140944—
Product(R)-2,6-Difluoro-4-difluoromethoxybenzyl 2-methylpiperazine-1-carboxylate fumarateHCID 21021906—

Reaction Steps

(R)-2,6-Difluoro-4-difluoromethoxybenzyl 2-methylpiperazine-1-carboxylate fumarate was prepared from 2,6-difluoro-4-difluoromethoxybenzyl alcohol and (R) 1-chlorocarbonyl-2-methyl-4-tert-butoxycarbonylpiperazine according to the methods described for Examples 54 to give the product as a white solid (2.9%); HPLC (XTERRA, 50/80, 220 nm) 86.0% (1.55 min); NMR δH (400 MHz, DMSO-d6) 1.154(3H, d, J 7.0 Hz), 2.639(1H, bm), 2.863(2H, bm), 3.007(2H, bm), 3.714(1H, bd), 4.122(1H, bs), 5.106(2H, q), 6.590(2H, s), 7.108(2H, d, J 8.5 Hz) and 7.360(1H, t, J 73 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022707B2
Source datasetuspto-grants-2006_04
ORD IDord-65257b6269064f838d395e6d8a3a4749
Source noteuspto-grants-2006_04