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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171728Generated: November 2, 2026

Acetic Anhydride → HCID 86609466, compound

https://huagongshe.com/reaction/1171728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 23138682HCID 23138682—
SolventDichloromethaneHCID 6344—
ProductHCID 86609466HCID 8660946671%

Reaction Steps

To a solution of (E)-3-{[1-(carboxymethyl)-1H-imidazol-2-yl]methylidene}-1-[2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]-4-sulfanylpiperidine hydrochloride (85.6 mg) in dichloromethane (4 ml) were added triethylamine (120 μl) and acetic anhydride (80 μl) at 0° C. After the mixture was stirred at room temperature for 3 hours, solvents were removed under reduced pressure and the residue was purified by silica gel chromatography using methanol and dichloromethane (5:95 to 25:75) as eluents to afford the free base of the title compound (57.7 mg, yield: 71%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-9a518afa87ab486593c3022e97d7e5ad
Source noteuspto-grants-2010_11