HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232579Generated: October 30, 2026
2,6-Dichloropyrazine → 2-Chloro-6-[4-(2,3-dihydro-1,4-benzodioxin-2-ylmethyl)-1-piperazinyl]pyrazine
https://huagongshe.com/reaction/2232579
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dichloropyrazine | HCID 78504 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(1,4-Benzodioxan-2-ylmethyl)piperazine | HCID 410682 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Chloro-6-[4-(2,3-dihydro-1,4-benzodioxin-2-ylmethyl)-1-piperazinyl]pyrazine | HCID 14371341 | 61.4% |
Reaction Steps
1-(2,3-Dihydro-1,4-benzodioxin-2-ylmethyl)piperazine (4.7 g, 20 mmole) and 2,6-dichloropyrazine (3.0 g, 20 mmole) were combined in 200 ml of dimethylformamide and 2.6 g (20 mmole) of diisopropylethylamine was added. The mixture was heated under nitrogen at 60° C. for 24 hours. The solvent was then removed in vacuum and the residue filtered through 75 g of silica gel with chloroform as the eluent. The product-containing fractions were concentrated in vacuum and the residue was crystallized from methanol with addition of 4N isopropanolic HCl and recrystallized from methanol to give 4.26 g of the title compound as the monohydrochloride, m.p. 270°-280° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04788290 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-9471c9d934044d948908ce99230571ed |
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| Source note | uspto-grants-1988_11 |
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