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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109974Generated: October 30, 2026

O-Xylene → N-(5-(1-(4-Acetoxytetrahydrofuran-3-yloxycarbonyl)ethylamino)-4-chloro-2-fluorophenyl)-3,4,5,6-tetrahydrophthalimide

https://huagongshe.com/reaction/1109974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(3-amino-4-chloro-6-fluorophenyl)-3,4,5,6-tetrahydrophthalimideHCID 15590180—
Reactant4-Acetoxytetrahydrofuran-3-yl 2-bromopropionateHCID 20078949—
SolventEthyl AcetateHCID 8857—
ProductN-(5-(1-(4-Acetoxytetrahydrofuran-3-yloxycarbonyl)ethylamino)-4-chloro-2-fluorophenyl)-3,4,5,6-tetrahydrophthalimideHCID 2007893532.9%

Reaction Steps

A mixture of 8.84 g of N-(5-amino-4-chloro-2-fluorophenyl)-3,4,5,6-tetrahydrophthalimide, 12.6 g of 4-acetoxytetrahydrofuran-3-yl 2-bromopropionate, 3.02 g of sodium hydrogencarbonate and 3 ml of xylene was heated under stirring at 150° to 160° C. for 4 hours. Adding ethyl acetate to the reaction mixture while it remained warm, the resulting mixture was washed with water, subsequently with aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by chromatography on a silica gel column (development solvent: ethyl acetate/hexane=1/2), to obtain 4.88 g of a compound described in Table 1 (No. 10) (33 %).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324709
Source datasetuspto-grants-1994_06
ORD IDord-102a3a40d1594100a84e2af56f2007a6
Source noteuspto-grants-1994_06