HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512773Generated: November 4, 2026
Sulfoxonium, trimethyl-, iodide (1:1) → HCID 58222469, compound
https://huagongshe.com/reaction/1512773
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 59146049 | HCID 59146049 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 58222469 | HCID 58222469 | — |
Reaction Steps
To a suspension of trimethylsulfoxonium iodide (132 mg) in DMSO (3 mL) stirred under nitrogen at 20° C. was added NaHMDS (1.0 mol/L in THF, 0.6 mL) dropwise during 5 mins. The reaction mixture was stirred at this temperature for 15 mins. A solution of ethyl (2E)-3-[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-methyl-1H-indol-3-yl]-2-propenoate (D62) (140 mg) in DMSO was added dropwise. After addition was complete, the reaction was stirred at room temperature for 1.5 h, and then warmed to 50° C. for 2 h. The reaction mixture was cooled to room temperature and partitioned between ethyl acetate (25 mL) and water (25 mL). The organic phase was washed with water, aqueous HCl (2 M) and brine, dried over sodium sulphate and evaporated to afford ethyl (1R,2R)-2-[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-methyl-1H-indol-3-yl]cyclopropanecarboxylate (D64) (80 mg). MS (ES): C26H26ClN3O4 requires 479. found 480.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08217028B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-0ce414a9fccf4a60a49a23c11799d6a3 |
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| Source note | uspto-grants-2012_07 |
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