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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653965Generated: October 29, 2026

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

https://huagongshe.com/reaction/1653965

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 numberUS05405828
Source datasetuspto-grants-1995_04
ORD IDord-653fee0bc36d4b6ba4be69ed5419edd7
Source noteuspto-grants-1995_04