HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417421Generated: October 27, 2026
Lawesson's reagent → 2-[5-(4-Bromo-phenyl)-thiazol-2-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/417421
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | 2-[2-(4-Bromo-phenyl)-2-oxo-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 58310150 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[5-(4-Bromo-phenyl)-thiazol-2-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 66620801 | 65.6% |
Reaction Steps
The mixture of 2-[2-(4-Bromo-phenyl)-2-oxo-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (1.0 g, 2.44 mmol) and Lawesson's reagent (1.23 g, 3.0 mmol) in THF (16 ml) was heated at 80° C. for 4 hours. The solvent was removed under reduced pressure and the mixture was diluted with EtOAc. The organic phase was washed with saturated sodium bicarbonate, water, and brine, and was dried with sodium sulfate. Concentration and purification by flash column chromatography (hexanes/EtOAc) gave 2-[5-(4-Bromo-phenyl)-thiazol-2-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester (655 mg). m/z: 410.7 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088368B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-75a9f1f55408487dbab72fc5eb3c36e4 |
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| Source note | uspto-grants-2012_01 |
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