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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13410Generated: October 26, 2026

2-Pyrazinecarboxylic acid → t-Butyl 2-(2-fluoro-4-((pyrazin-2-ylcarbonyl)amino)phenyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/13410

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Pyrazinecarboxylic acidHCID 1047—
ReactantPyridineHCID 1049—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactantt-Butyl 2-(4-amino-2-fluoro-phenyl)-pyrrolidine-1-carboxylateHCID 23145592—
SolventChloroformHCID 6212—
Productt-Butyl 2-(2-fluoro-4-((pyrazin-2-ylcarbonyl)amino)phenyl)pyrrolidine-1-carboxylateHCID 23145269—

Reaction Steps

1.5 g of pyrazine-2-carboxylic acid and 3.1 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide monohydrochloride were added to a pyridine (50 ml) solution of 3 g of t-butyl 2-(4-amino-2-fluoro-phenyl)-pyrrolidine-1-carboxylate obtained in Example 338 (step 2), and the reaction liquid was stirred at room temperature for 3 hours. The reaction liquid was diluted with chloroform, washed with water and saturated saline in order, and dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: chloroform/methanol=50/1) to obtain the entitled compound as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728025B2
Source datasetuspto-grants-2010_06
ORD IDord-a9d1f97d113b42dda6ccf4e0de999b2f
Source noteuspto-grants-2010_06