HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765082Generated: October 26, 2026
(R)-2-Chloro-3-(2-methylpiperazin-1-YL)pyrazine → 2-[2-(2-[2-(Dimethylamino)ethoxy]phenoxy)ethoxy]-3-[(2R)-2-methylpiperazin-1-yl]pyrazine
https://huagongshe.com/reaction/1765082
Participants
| Role | Name | HCID | Charge |
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| Reactant | (R)-2-Chloro-3-(2-methylpiperazin-1-YL)pyrazine | HCID 9992195 | — |
| Reactant | 2-{2-[2-(Dimethylamino)ethoxy]phenoxy}ethanol | HCID 21106655 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[2-(2-[2-(Dimethylamino)ethoxy]phenoxy)ethoxy]-3-[(2R)-2-methylpiperazin-1-yl]pyrazine | HCID 10386333 | 60% |
Reaction Steps
To a solution of 2-{2-[2-(dimethylamino)ethoxy]phenoxy}ethanol (from Step 3; 0.82 g, 3.6 mmol) in dry DMF (25 mL) was added potassium tert-butoxide (0.59 g, 5.3 mmol) and the mixture was stirred at room temperature for 10 minutes. To the mixture was added 2-chloro-3-[(2R)-2-methylpiperazin-1-yl]pyrazine* (0.70 g, 3.3 mmol) in DMF (5 mL) in one portion and the reaction mixture was stirred at 55° C. for 2 h. A small spoon of silica was added, the solvent was filtered off and the solvent was evaporated under reduced pressure. The crude product was purified on a column of silica (100 mm, i.d.=30 mm) with CHCl3/MeOH/NH4OH (95:5:0.2; 100 mL, followed by 90:10:0.2) as eluent to give 0.80 g (60%) of the title compound as a light brown oil. HRMS m/z calcd for C21H31N5O3 (M)+ 401.2427. found 401.2414. *Reported in WO 00/76984, Example 192, Step 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07226925B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-158a6e7d631c47b69b7cd7bee3e7174d |
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| Source note | uspto-grants-2007_06 |
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