HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556680Generated: October 31, 2026
Potassium Carbonate → HCID 178490673, compound
https://huagongshe.com/reaction/556680
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | [(2S)-5-oxopyrrolidin-2-yl]methyl 4-methylbenzene-1-sulfonate | HCID 2734055 | — |
| Reactant | n-(5-Tert-butylthiazol-2-yl)-5-chloro-2-methoxybenzamide | HCID 87094486 | — |
| Catalyst | Tetraethylammonium Iodide | HCID 6225 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178490673 | HCID 178490673 | 48.5% |
Reaction Steps
A mixture of Example 4C (810 mg, 2.49 mmol), (S)-(5-oxopyrrolidin-2-yl)methyl 4-methylbenzenesulfonate (Aldrich, 807 mg, 3 mmol), potassium carbonate (828 mg, 6 mmol), tetrabutylammonium iodide (20 mg, 0.05 mmol), tetrabutylammonium hydrogensulfate (20 mg, 0.06 mmol) and tetraethylammonium iodide (20 mg, 0.07 mmol) in anhydrous toluene (100 mL) was refluxed for 15 h. The mixture was cooled to room temperature, washed with water, brine, dried with anhydrous MgSO4, filtered, and concentrated under reduced pressure. The residue was chromatographed (SiO2, ethyl acetate-ethanol 9:1) to afford 510 mg of the title compound. 1H NMR (300 MHz, DMSO-d6) δ 1.32 (s, 9H), 1.83 (m, 1H), 2.07 (m, 3H), 3.78 (s, 3H), 4.09 (m, 2H), 4.30 (m, 1H), 7.10 (d, J=9 Hz, 1H), 7.27 (s, 1H), 7.45 (dd, J=9 Hz, 3 Hz, 1H), 7.62 (d, J=3 Hz, 1H), 7.82 (broad s, 1H); MS (DCI/NH3) m/z 422 (M+H)+. Anal. calcd for C20H24ClN3O3S.0.25 H2O: C, 56.33; H, 5.79; N, 9.85. Found: C, 56.42; H, 5.55; N, 9.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058293B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-0f3d241b7e534524a01ca6de7cb2ba63 |
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| Source note | uspto-grants-2011_11 |
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