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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichloropyrazineHCID 78575—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 178497919HCID 178497919—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(amino(3-chloropyrazin-2-yl)methyl)benzoateHCID 9030349381.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446130B2
Source datasetuspto-grants-2016_09
ORD IDord-f78ef12cdd7844ecb1edb41d70388ec3
Source noteuspto-grants-2016_09