Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483Generated: October 26, 2026

Ethyl Acetate → N-{4-Chloro-2-fluoro-5-[hexahydro-2,4,6,-trioxo-3-(2-propynyl)-s-triazin-1-yl]phenyl}-1-cyclohexene-1,2-dicarboximide

https://huagongshe.com/reaction/1483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
Reactant1-(5-Amino-2-chloro-4-fluorophenyl)-3-(2-propynyl)-s-triazine-2,4,6-(1H,3H,5H)-trioneHCID 19690738—
SolventAcetic AcidHCID 176—
ProductN-{4-Chloro-2-fluoro-5-[hexahydro-2,4,6,-trioxo-3-(2-propynyl)-s-triazin-1-yl]phenyl}-1-cyclohexene-1,2-dicarboximideHCID 13171989755.9%

Reaction Steps

A solution of 1-(5-amino-2-chloro-4-fluorophenyl)-3-(2-propynyl)-s-triazine-2,4,6-(1H,3H,5H)-trione (1.50 g, 4.83 mmol), and 3,4,5,6-tetrahydrophthalic anhydride (0.73 g, 4.83 mmol) in acetic acid (3 mL) is heated at 100° C. for 5 hours, cooled, and poured into ethyl acetate, The organic mixture is washed sequentially with water, saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a yellow semi-solid. Flash column chromatography of the semi-solid using silica gel and an ethyl acetate/hexanes (1:2) solution gives the title product as a white solid (1.20 g, mp 127°-135° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726126
Source datasetuspto-grants-1998_03
ORD IDord-9fc8235e42584d779056ec0da7bbdc76
Source noteuspto-grants-1998_03