HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62453Generated: October 27, 2026
2,3-Dichloropyrazine → Methyl 4-(amino(3-chloropyrazin-2-yl)methyl)benzoate
https://huagongshe.com/reaction/62453
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dichloropyrazine | HCID 78575 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 178497919 | HCID 178497919 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-(amino(3-chloropyrazin-2-yl)methyl)benzoate | HCID 90303493 | 81.2% |
Reaction Steps
To a solution of (E)-methyl 4-((benzhydrylimino)methyl)benzoate (67 g, 204 mmol) in THF (700 mL) was cooled to 0° C. and added dropwise NaHMDS (244 mL, 244 mmol). The mixture was stirred at this temperature for 30 minutes, and added a solution of 2,3-dichloropyrazine (33.2 g, 224 mmol) in THF (40 mL). The reaction mixture was stirred at 0° C. for 20 minutes and RT for 40 minutes. After the reaction was completed, the reaction mixture was extracted with EA and water. The organic layer was treated with 3M HCl (500 mL) for 10 minutes. The phases were separated and the organic layer was extracted with 3M HCl. The aqueous was washed with EA and then alkalified with Na2CO3 to pH=9. The aqueous solution was extracted with EA and the combined organics were dried and concentrated to give methyl 4-(amino(3-chloropyrazin-2-yl)methyl)benzoate (46 g, yield 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09446130B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-f78ef12cdd7844ecb1edb41d70388ec3 |
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| Source note | uspto-grants-2016_09 |
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