HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051901Generated: November 1, 2026
Potassium Carbonate → 1-((4-(4-Chlorophenyl)thiazol-2-yl)methyl)pyrrolidin-2-one
https://huagongshe.com/reaction/1051901
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chlorophenylboronic acid | HCID 74299 | — |
| Reactant | 4-(4-(4-Chlorophenyl)-2-((2-oxopyrrolidin-1-yl)methyl)thiazol-5-yl)benzenesulfonamide | HCID 71735399 | — |
| Reactant | HCID 89813516 | HCID 89813516 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-((4-(4-Chlorophenyl)thiazol-2-yl)methyl)pyrrolidin-2-one | HCID 89813335 | 86.6% |
Reaction Steps
(4-chlorophenyl) boronic acid (0.22 g, 1.42 mmol) and potassium carbonate (0.41 g, 2.97 mmol) were added to a solution of 1-((4-bromothiazol-2-yl)methyl)pyrrolidin-2-one (Step-1 of Compound 103, 0.31 g, 1.18 mmol) in a mixture of toluene:ethanol (5:15 ml) in a tube at 25° C. Nitrogen gas was bubbled through the reaction mixture for 15 minutes. Tetrakis(triphenylphosphine)(0)palladium (0.07 g, 0.06 mmol) was then added to the reaction mixture under nitrogen atmosphere and the tube was sealed. The reaction mixture was heated at 95-100° C. for lhr under stirring. The progress of the reaction was monitored by TLC. The reaction mixture was then cooled to 25° C. and filtered through celite. The celite cake was washed with ethanol (20 ml). The combined filtrate was concentrated under reduced pressure to obtain a crude product, which was then purified by column chromatography using 40% ethyl acetate in hexanes as an eluent to obtain the title compound (0.3 g, 86.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388196B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-a97c1b8094254b22a7901fc5afea14ec |
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| Source note | uspto-grants-2016_07 |
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