HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188930Generated: October 31, 2026
Lawesson's reagent → HCID 86652848, compound
https://huagongshe.com/reaction/1188930
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 66897756 | HCID 66897756 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86652848 | HCID 86652848 | 98.3% |
Reaction Steps
To a solution of 7-[2-methoxy-1-(methoxymethyl)ethoxy]-5-{[5-(methylsulfonyl)pyridin-2-yl]oxy}-1H-indole-2-carboxamide (1.66 g) in tetrahydrofuran (40 mL) was added Lawesson's reagent (1.5 g), and the mixture was stirred at 50° C. for 2 h. Lawesson's reagent (0.5 g) was added to the mixture again. After stirring at 50° C. for 1 h, the mixture was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and the mixture was washed with saturated brine, dried over magnesium sulfate, filtered and concentrated. The residue was purified by basic silica gel column chromatography (methanol/ethyl acetate/hexane=0/10/90 to 10/90/0, volume ratio) to give the title compound (1.69 g, 98%) as a yellow amorphous solid. MS 466 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673942B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-68ca239c38c2435a97d86c6444375dcd |
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| Source note | uspto-grants-2014_03 |
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