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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085211Generated: November 1, 2026

Acetic Anhydride → HCID 60078094, compound

https://huagongshe.com/reaction/2085211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 9913387HCID 9913387—
SolventPyridineHCID 1049—
ProductHCID 60078094HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720320B2
Source datasetuspto-grants-2004_04
ORD IDord-b3d782e29b944a01ab5135910f7966c4
Source noteuspto-grants-2004_04