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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201583Generated: October 29, 2026

4-Methylmorpholine → HCID 117772597, compound

https://huagongshe.com/reaction/2201583

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantEthyl chloroformateHCID 10928—
Reactant(1R)-(+)-1-(4-Fluorophenyl)ethylamineHCID 6950187—
ReactantHCID 117771339HCID 117771339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117772597HCID 11777259776%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(benzyloxy)-6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)picolinic acid (110 mg, 0.18 mmol) was suspended in THF (2 ml), cooled to 0° C., then 4-methylmorpholine (55.3 mg, 0.55 mmol) and ethylchloroformate (27.7 mg, 0.26 mmol) were added. The resulting mixture was stirred at 0° C. for 1 h, then (R)-1-(4-fluorophenyl)ethylamine was added. The reaction was warmed to RT and stirred for 1 h, then concentrated in vacuo. The resulting residue was purified using column chromatography (eluted with 0-5% MeOH/DCM) to provide (R)-3-(benzyloxy)-6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)-N-(1-(4-fluorophenyl)ethyl)picolinamide (100 mg, yield: 76%). MS (M+H)+: 724.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364482B2
Source datasetuspto-grants-2016_06
ORD IDord-fd0bd1345ee14231aa0d769a298fd3cc
Source noteuspto-grants-2016_06