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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467783Generated: October 30, 2026

Dimethylformamide → Methyl 3-(bis(tert-butoxycarbonyl)amino)-6-pyrrolidin-1-yl-pyrazine-2-carboxylate

https://huagongshe.com/reaction/467783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
ReactantPyrrolidineHCID 31268—
ReactantMethyl 3-(bis(tert-butoxycarbonyl)amino)-6-bromopyrazine-2-carboxylateHCID 86660188—
CatalystBinolHCID 11762—
Catalystcopper(I) bromideHCID 24593—
SolventWaterHCID 962—
ProductMethyl 3-(bis(tert-butoxycarbonyl)amino)-6-pyrrolidin-1-yl-pyrazine-2-carboxylateHCID 7009856075.5%

Reaction Steps

A pre-dried flask was charged with copper(I) bromide (0.35 mg, 2.89 μmol), (R)-(+)-1,1′-bi-2-naphthol (1.66 mg, 5.78 μmol) and cesium carbonate (113 mg, 347 μmol) under argon atmosphere. DMF (0.5 ml), methyl 3-(bis(tert-butoxycarbonyl)amino)-6-bromopyrazine-2-carboxylate (50 mg, 116 μmol) and pyrrolidine (14.3 μl, 174 μmol) were added and the reaction mixture was stirred at r.t. for 1.5 h. The reaction mixture was poured into water (10 ml) and extracted with ethyl acetate. The combined organic layer was washed with brine, dried, evaporated and purified by silica gel chromatography using a heptane/ethyl acetate gradient to yield the product as yellow solid (37 mg, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623866B2
Source datasetuspto-grants-2014_01
ORD IDord-d8a86a22568446cbb0ceb3e1fa1820b6
Source noteuspto-grants-2014_01