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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 2-Amino-6-Bromo-4-Methoxyphenol | HCID 11171982 | — |
| Reactant | Ethylcarbodiimide | HCID 12973440 | — |
| Reactant | DL-5 oxo-pyrrolidine-2-carboxylic acid | HCID 131725757 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Oxo-pyrrolidine-2-carboxylic acid (3-bromo-2-hydroxy-5-methoxy-phenyl)-amide | HCID 86592454 | 102.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045539B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-80eb094478c94e89a16c10eca3950c1f |
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| Source note | uspto-grants-2006_05 |
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