HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469744Generated: October 29, 2026
Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → HCID 67953418, compound
https://huagongshe.com/reaction/469744
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | HCID 67953843 | HCID 67953843 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67953418 | HCID 67953418 | — |
| Product | HCID 67953843 | HCID 67953843 | — |
Reaction Steps
(S)-5-Oxo-1-(4-trifluoromethyl-phenyl)-pyrrolidine-2-carboxylic acid {3-[1,1-dimethyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-isoxazol-5-yl}-amide is synthesized in a similar manner as Example 16, Method 7. (S)-5-Oxo-1-(4-trifluoromethyl-phenyl)-pyrrolidine-2-carboxylic acid {3-[1,1-dimethyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-isoxazol-5-yl}-amide (0.546 g; 1.103 mmol) is dissolved in 2 mL ethanol and pyridinium p-toluenesulfonate (0.055 g; 0.221 mmol) is added. The mixture is heated at 55° C. for 4 h and then concentrated and purified by reverse phase HPLC to afford title compound. ESI m/z 412 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629157B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-c307b4b5efc34d149ca8500540b44562 |
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| Source note | uspto-grants-2014_01 |
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