HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048533Generated: October 31, 2026
2-Thiophenesulfonamide → HCID 67999458, compound
https://huagongshe.com/reaction/1048533
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Thiophenesulfonamide | HCID 72881 | — |
| Reactant | Cyanomethylenetributylphosphorane | HCID 4622928 | — |
| Reactant | HCID 67999735 | HCID 67999735 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67999458 | HCID 67999458 | — |
Reaction Steps
To a solution of methyl 2-((3R,5R,6S)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-((S)-1-cyclopropyl-2-hydroxyethyl)-3-methyl-2-oxopiperidin-3-yl)acetate (100 mg, 0.184 mmol; Example 263, Step C) and cyanomethylenetributylphosphorane (177 μL, 0.734 mmol) in toluene (0.92 mL) was added thiophene-2-sulfonamide (90 mg, 0.55 mmol) and the resulting solution was stirred at 35° C. overnight. The reaction was quenched (sat. NH4Cl), extracted (2×EtOAc), and washed (brine). The combined organic layers were dried (Na2SO4) and concentrated under the reduced pressure. Purification of the residue by chromatography on silica gel (24 g SiO2, 35% EtOAc/Hex) provided the title compound as a pale yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569341B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-fa049b4e1b934cf3ad6165ca77eed6ef |
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| Source note | uspto-grants-2013_10 |
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