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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064307Generated: October 30, 2026

2-(1,3-Dioxoisoindolin-2-yl)ethyl trifluoromethanesulfonate → 2-(3-Chloroanilino)-4-[1-(2-phthalimidoethyl)imidazol-5-yl]pyrimidine

https://huagongshe.com/reaction/1064307

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(1,3-Dioxoisoindolin-2-yl)ethyl trifluoromethanesulfonateHCID 11809465—
Reactant2-(3-Chloroanilino)-4-(1-triphenylmethylimidazol-4-yl)pyrimidineHCID 22273504—
SolventDichloromethaneHCID 6344—
Product2-(3-Chloroanilino)-4-[1-(2-phthalimidoethyl)imidazol-5-yl]pyrimidineHCID 2227350640%

Reaction Steps

2-Phthalimidoethyl triflate (660 mg, 2.04 mmol) was added to solution of the 2-(3-chloroanilino)-4-(1-triphenylmethylimidazol-4-yl)pyrimidine Method 2; 1.00 g, 1.95 mmol) in DCM (5 ml) and the reaction mixture stirred for 4 hours. The solvent was removed by evaporation and MeOH (6 ml) and 2M hydrochloric acid (1.5 ml) was added to the residue. The mixture was stirred for 5 minutes, the volatiles were removed by evaporation and the residue partitioned between EtOAc and saturated aqueous sodium hydrogen carbonate solution. The resulting precipitate was collected by filtration, washed with water and EtOAc and dried to give the title compound 350 mg, (40%) as a solid. NMR: 3.81-3.96 (m, 2H), 4.77-4.92 (m, 2H), 6.98 (d, 1H), 7.06 (d, 1H), 7.31 (t, 1H), 7.37 (d, 1H), 7.63-7.80 (m, 6H), 7.92 (s, 1H), 8.27 (d, 1H), 9.50 (s, 1H); m/z: 443.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969714B2
Source datasetuspto-grants-2005_11
ORD IDord-07c2d75e86964e0281dee757f53057c8
Source noteuspto-grants-2005_11