HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827148Generated: October 30, 2026
2,3-Dichloropyrazine → HCID 10134283, compound
https://huagongshe.com/reaction/1827148
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dichloropyrazine | HCID 78575 | — |
| Reactant | HCID 22135582 | HCID 22135582 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10134283 | HCID 10134283 | — |
Reaction Steps
To 2,3-dichloropyrazine (0.160 gm, 0.00107 mol) was added 4-fluorobenzyl 4-(aminomethyl)piperidine-1-carboxylate (INTERMEDIATE 2C) (0.86 gm, 0.00322 mol) and the resulting mixture heated under nitrogen at 110° C. for 30 min. The reaction was cooled, diluted with ethyl acetate (5 mL), and washed with 10% aqueous sodium/citric acid pH=5.2 (3×30 mL), and 10% aqueous sodium bicarbonate (30 mL). The ethyl acetate extract was dried over sodium sulfate, filtered through a pad of silica and concentrated to an oil. Crystallization from ether/hexane gave 4-[(3-chloro-pyrazin-2-ylamino)-methyl]-piperidine-1-carboxylic acid 4-fluoro-benzyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053089B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-e98228a0c13340f99342ed5fd9fe5ae0 |
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| Source note | uspto-grants-2006_05 |
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