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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724826Generated: November 1, 2026

Pyridine → HCID 21100628, compound

https://huagongshe.com/reaction/1724826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 21100634HCID 21100634—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21100628HCID 2110062828%

Reaction Steps

To the suspension of 2-{1-Amino-5-[4-(4-fluoro-benzyl)-piperidine-1-carbonyl]-6-methoxy-1H-indol-3-yl}-N,N-dimethyl-2-oxo-acetamide (100 mg, 0.21 mmol) in anhydrous THF (3 mL) was added pyridine (60 uL, 0.63 mmol) and acetyl chloride (45 uL, 0.63 mmol) at 0° C. The mixture became clear and was stirred continually at RT for 72 h. The reaction mixture was evaporated in vacuo. The crude material was added water and it was extracted with CH2Cl2. The organic extract was dried (Na2SO4), filtered, and concentrated. The residue was purified by radial chromatography with 0-3% MeOH/CHCl3 to give 30 mg (28% ) of the desired product. M+H+ (523).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488744B2
Source datasetuspto-grants-2009_02
ORD IDord-62863f95a8314099be32b08782f4242d
Source noteuspto-grants-2009_02