HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460640Generated: October 29, 2026
Acetic Anhydride → HCID 60078094, compound
https://huagongshe.com/reaction/460640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 9913387 | HCID 9913387 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 60078094 | HCID 60078094 | — |
Reaction Steps
(S)-4-(2-Hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)-N-methoxy-N-methylbenzo(b)furan-2-carboxamide (0.40 g) obtained in Example 6 was dissolved in pyridine (20 ml) and acetic anhydride (10 ml) was added at room temperature. The mixture was stood for one day. The solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (chloroform/methanol) to give (S)-4-(2-acetoxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)-N-methoxy-N-methylbenzo(b)furan-2-carboxamide (0.34 g) as a brown oil. This was dissolved in ethanol and maleic acid (0.10 g) was added. The precipitated crystals were collected by filtration and dried to give the title compound (0.25 g) as pale-yellow crystals, melting point 125–127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196199B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-f54caee500de4784aa0dbaa70564225a |
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| Source note | uspto-grants-2007_03 |
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