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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877518Generated: October 26, 2026

2-Fluoroethylamine → 2-methylpropan-2-yl 4-[4-(6-cyanopyridin-3-yl)-9H-carbazol-9-yl]-2-[(2-fluoroethyl)amino]benzoate

https://huagongshe.com/reaction/1877518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoroethylamineHCID 9996—
ReactantPotassium CarbonateHCID 11430—
Reactant2-methylpropan-2-yl 4-[4-(6-cyanopyridin-3-yl)-9H-carbazol-9-yl]-2-fluorobenzoateHCID 58338293—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product2-methylpropan-2-yl 4-[4-(6-cyanopyridin-3-yl)-9H-carbazol-9-yl]-2-[(2-fluoroethyl)amino]benzoateHCID 8665516619.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

4.83 g of potassium carbonate and 3 g (40 mmol) of 2-fluoroethylamine are successively added to a solution of 0.7 g of 2-methylpropan-2-yl 4-[4-(6-cyanopyridin-3-yl)-9H-carbazol-9-yl]-2-fluorobenzoate, obtained in stage 1 of Example 49, in 5 ml of dimethyl sulphoxide. The reaction mixture is heated at 90° C. for 2 hours and 50 minutes in a microwave, and then diluted with distilled water. The aqueous phase is washed twice with ethyl acetate and the combined organic phases are washed with water and a saturated solution of sodium chloride, dried over magnesium sulphate and concentrated to dryness under reduced pressure. The residue is purified by silica gel chromatography, elution being carried out with dichloromethane, so as to give 0.15 g of 2-methylpropan-2-yl 4-[4-(6-cyanopyridin-3-yl)-9H-carbazol-9-yl]-2-[(2-fluoroethyl)amino]benzoate in the form of a white powder, the characteristics of which are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309721B2
Source datasetuspto-grants-2012_11
ORD IDord-fce5218875df45e6af178ccedc2fdd29
Source noteuspto-grants-2012_11