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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765091Generated: October 30, 2026

(R)-2-Chloro-3-(2-methylpiperazin-1-YL)pyrazine → 2-{2-[{2-[3-(Dimethylamino)propyl]pyridin-3-yl}oxy]ethoxy}-3-[(2R)-2-methylpiperazin-1-yl]pyrazine

https://huagongshe.com/reaction/1765091

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-2-Chloro-3-(2-methylpiperazin-1-YL)pyrazineHCID 9992195—
Reactant2-({2-[3-(Dimethylamino)propyl]pyridin-3-yl}oxy)ethanolHCID 21106663—
Product2-{2-[{2-[3-(Dimethylamino)propyl]pyridin-3-yl}oxy]ethoxy}-3-[(2R)-2-methylpiperazin-1-yl]pyrazineHCID 1045362858%

Reaction Steps

The procedure in Example 18, Step 4, starting from 2-chloro-3-[(2R)-2-methylpiperazin-1-yl]pyrazine* (0.48 g, 2.28 mmol) and 2-({2-[3-(dimethylamino)propyl]pyridin-3-yl}oxy)ethanol (from Step 1; 0.46 g, 2.07 mmol) was followed. The crude product was purified on a column of silica (100 mm, i.d.=30 mm) with CHCl3/MeOH/NH4OH (80:20:0.5; 200 mL, followed by 60:40:1) as eluent to give 0.48 g (58%) of the title compound as a colorless oil. HRMS m/z calcd for C21H32N6O2 (M)+ 400.2587. found 400.2571. *Reported in WO 00/76984, Example 192, Step 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226925B2
Source datasetuspto-grants-2007_06
ORD IDord-10935df990804821969e9c0268eee654
Source noteuspto-grants-2007_06