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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797318Generated: October 25, 2026

Hydrochloric Acid → 1-(2-{[3-Chloro-4-(2-methylbenzoyl)phenyl]amino}phenyl)pyrrolidine-2,5-dione

https://huagongshe.com/reaction/1797318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-[2-[3-Chloro-4-(2-methylbenzoyl)-phenylamino]phenyl]-succinamic AcidHCID 9845903—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(2-{[3-Chloro-4-(2-methylbenzoyl)phenyl]amino}phenyl)pyrrolidine-2,5-dioneHCID 22174456—

Reaction Conditions

Temperature-15 °C

Reaction Steps

Iso-butylchloroformate (60 μL, 0.46 mmol) was added to a stirred solution of N-(2-{[3-chloro-4-(2-methylbenzoyl)phenyl]amino}phenyl)-succinamic acid (200 mg, 0.46 mmol) (disclosed in WO 01/05746) and 4-methylmorpholine (51 μL, 0.46 mmol) in THF (5.0 mL) at −15° C. After 5 min at 0° C. the reaction mixture was cooled to −15° C. and a solution of ethyl diisopropyl amine (65 μL, 0.46 mmol) in THF (5.0 mL) was added. The resulting reaction mixture was kept at 0° C. for 1 h. The reaction mixture was stirred for 16 h at RT and then poured into a mixture of 1 M HCl(aq) and EtOAc. The organic phase was washed with more HCl(aq)(×2). The organic phase was washed with brine, dried (MgSO4), filtered and concentrated in vacuo. The crude product was purified by flash chromatography using petroleum ether/EtOAc 1:2 as the eluent to afford the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034015B2
Source datasetuspto-grants-2006_04
ORD IDord-76dee2b40dd6468d9a349eeade00fdd4
Source noteuspto-grants-2006_04