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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352807Generated: November 1, 2026

Pyridine → HCID 21100628, compound

https://huagongshe.com/reaction/1352807

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 numberUS07220763B2
Source datasetuspto-grants-2007_05
ORD IDord-978b8be5a18246d4b27b73c2acf0db1f
Source noteuspto-grants-2007_05