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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626718Generated: November 1, 2026

Potassium Carbonate → [4-(2-morpholin-4-yl-4-oxo-4H-chromen-8-yl)-benzyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1626718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(tert-Butoxycarbonylaminomethyl)phenylboronic acidHCID 3863163—
Reactanttrifluoro-methanesulfonic acid 2-morpholin-4-yl-4-oxo-4H-chromen-8-yl esterHCID 11603298—
Solvent1,4-DioxaneHCID 31275—
Product[4-(2-morpholin-4-yl-4-oxo-4H-chromen-8-yl)-benzyl]-carbamic acid tert-butyl esterHCID 66685659—

Reaction Conditions

Temperature80 °C

Reaction Steps

Trifluoro-methanesulfonic acid 2-morpholin-4-yl-4-oxo-4H-chromen-8-yl ester [E] (380 mg, 1.0 mmol), 4-(N-Boc-aminomethyl)phenylboronic acid (280 mg, 1.1 mmol, 1.1 eq), potassium carbonate (275 mg, 2.0 mmol, 2 eq) and tetrakis triphenylphosphine palladium (0) (60 mg, 0.05 mmol 0.05 eq) were stirred in dioxane (4 ml) and heated to 80° C. for 4 hours. The cooled reaction was then filtered and the filtrate concentrated in vacuo. The residue was purified by flash chromatography eluting with 0-3% methanol in dichloromethane to afford [4-(2-morpholin-4-yl-4-oxo-4H-chromen-8-yl)-benzyl]-carbamic acid tert-butyl ester [F]. Yield 238 mg, 54%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785457B2
Source datasetuspto-grants-2014_07
ORD IDord-43c16441137a409e91c9ebd9967789b9
Source noteuspto-grants-2014_07