HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504682Generated: October 28, 2026
Triphenylphosphine Oxide → HCID 59135917, compound
https://huagongshe.com/reaction/504682
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine Oxide | HCID 13097 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 59136130 | HCID 59136130 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 59135917 | HCID 59135917 | 57% |
Reaction Steps
To a solution of triphenylphosphine oxide (1.00 g) in acetonitrile (20 ml) was slowly added trifluoromethanesulfonic anhydride (0.30 ml) at 0° C., and the mixture was stirred for 10 min. N-[2-(Benzylthio)-2-methyl-3-(morpholino)propyl]-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamide (0.43 g) was added, and the reaction mixture was stirred at 0° C. for 30 min. Saturated aqueous sodium hydrogencarbonate was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The residue was subjected to silica gel column chromatography to give the title compound (0.20 g, yield 57%) as colorless crystals from a fraction eluted with ethyl acetate-hexane (2:1, volume ratio). melting point 146-147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07777047B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-506b4dbb85e1473a9ccf8ffce98741ca |
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| Source note | uspto-grants-2010_08 |
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