HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451357Generated: October 25, 2026
Hydrochloric Acid → HCID 45380782, compound
https://huagongshe.com/reaction/451357
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (4S,5S)-4,5-dimethyl-1,3,2-dioxathiolane 2,2-dioxide | HCID 13545565 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 4-Methyl-N-(4-(methylsulfonyl)phenyl)-5-(2-(trifluoromethyl)phenyl)-1H-pyrrole-3-carboxamide | HCID 58538830 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 45380782 | HCID 45380782 | 69% |
Reaction Steps
To a solution of 4-methyl-N-[4-(methylsulfonyl)phenyl]-5-[2-(trifluoromethyl)phenyl]-1H-pyrrole-3-carboxamide (28 g, 66 mmol) in anhydrous N,N-dimethylacetamide (DMA) (0.53 L) was added sodium tert-butoxide (15 g, 15 mmol) and stirred at room temperature for 30 min under N2. (4S,5S)-4,5-dimethyl-1,3,2-dioxathiolane 2,2-dioxide (15 g, 99 mmol) in anhydrous DMA (2.0 ml) was added to the solution and stirred at 70° C. for 2.0 h. The reaction mixture was cooled to room temperature and added 2N HCl (0.14 L) and concentrated on a rotary evaporator. To this residue was added anhydrous tetrahydrofuran (THF) (140 ml) and 5N HCl (0.14 L) and stirred at 60° C. for 90 min. The mixture was diluted with ethyl acetate and washed with water, saturated NaHCO3 and brine, then dried over sodium sulfate and concentrated on a rotary evaporator. The resulting residue was purified by silica-gel column chromatography (9:1 to 1:1 dichloromethane:ethyl acetate) to give an atropisomeric mixture of title compound as a white solid (22.5 g, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08487117B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-8f9bdc5e51bf4f3b977a9f899c9f11fb |
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| Source note | uspto-grants-2013_07 |
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