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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41217Generated: October 27, 2026

HCID 86672436, compound → tert-butyl 2-(6-(methoxycarbonyl)-2-((R)-2-methylmorpholino)-4-oxo-4H-chromen-8-yl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/41217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86672436HCID 86672436—
CatalystRhodiumHCID 23948—
SolventMethanolHCID 887—
Producttert-butyl 2-(6-(methoxycarbonyl)-2-((R)-2-methylmorpholino)-4-oxo-4H-chromen-8-yl)pyrrolidine-1-carboxylateHCID 8667243759%

Reaction Steps

(R)-tert-Butyl 2-(6-(methoxycarbonyl)-2-(2-methylmorpholino)-4-oxo-4H-chromen-8-yl)-1H-pyrrole-1-carboxylate (2 g, 4.27 mmol) and 5% Rhodium on Alumina (50% wet) (0.4 g, 0.09 mmol) in MeOH (50 mL) were stirred under an atmosphere of hydrogen at 5 bar and 65° C. for 2 h. More catalyst was added and stirring continued overnight. 2 g of 5% Rh/C was then added followed by the same amount after 1 h then after another 2 h. The catalyst was filtered through celite and washed with MeOH/DCM and the solvent evaporated. The crude product was purified by flash chromatography on silica gel eluting with 10 to 15% MeOH in EtAc. The solvent was evaporated to dryness to afford tert-butyl 2-(6-(methoxycarbonyl)-2-((R)-2-methylmorpholino)-4-oxo-4H-chromen-8-yl)pyrrolidine-1-carboxylate (1.18 g, 59%) as a white solid. Mass Spectrum: m/z [M+H]+=473.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530470B2
Source datasetuspto-grants-2013_09
ORD IDord-b857934df5194e0d921e9780b344244e
Source noteuspto-grants-2013_09