Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824793Generated: November 2, 2026

2-Dimethylaminopyridine → 5-Oxo-pyrrolidine-2-carboxylic acid (3-bromo-2-hydroxy-5-methoxy-phenyl)-amide

https://huagongshe.com/reaction/1824793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-DimethylaminopyridineHCID 21885—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-Amino-6-Bromo-4-MethoxyphenolHCID 11171982—
ReactantEthylcarbodiimideHCID 12973440—
ReactantDL-5 oxo-pyrrolidine-2-carboxylic acidHCID 131725757—
SolventDichloromethaneHCID 6344—
Product5-Oxo-pyrrolidine-2-carboxylic acid (3-bromo-2-hydroxy-5-methoxy-phenyl)-amideHCID 86592454102.3%

Reaction Steps

2-Amino-6-bromo-4-methoxy-phenol (0.40 g), 1,3-dimethylaminopropyl)-3-ethylcarbodiimide (1.06 g), 1-hydroxybenzotriazole (0.50 g), dimethylaminopyridine (0.22 g) and DL-5-oxo-pyrrolidine-2-carboxylic acid (0.25 g) were reacted together in methylene chloride (7.3 mL). After 3 h, the reaction was diluted with methylene chloride (10 mL) and washed successively with 1N HCl (10 mL), sat. aq. NaHCO3 (10 mL), sat. aq. NaCl (10 mL). The organic layer was dried over sodium sulfate, filtered through celite and concentrated. Chromatography on silica gel (eluant: 0 to 20% methanol:methylene chloride) afforded 5-oxo-pyrrolidine-2-carboxylic acid (3-bromo-2-hydroxy-5-methoxy-phenyl)-amide (0.18 g). MS: 370.2 (100%), 372.2 (90%) (MH+); HPLC tR: 1.51 min. 5-Oxo-pyrrolidine-2-carboxylic acid (3-bromo-2-hydroxy-5-methoxy-phenyl)-amide was cyclized according to synthetic method R to obtain the title compound (0.09 g) after purification on silica gel (eluant: 0 to 30% methanol:methylene chloride). MS: 352.2 (100%), 354.2 (95%) (MH++CH3CN), 311.2 (20%), 313.2 (20%) (MH+).; HPLC tR: 1.84 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045539B2
Source datasetuspto-grants-2006_05
ORD IDord-80eb094478c94e89a16c10eca3950c1f
Source noteuspto-grants-2006_05