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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109853Generated: October 30, 2026

Pyridine → HCID 54710418, compound

https://huagongshe.com/reaction/2109853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 131727396HCID 131727396—
SolventDichloromethaneHCID 6344—
ProductHCID 54710418HCID 54710418—

Reaction Steps

To a suspension of 2-(4-fluorobenzyl)-8,9-dihydroxy-7-(piperidin-4-ylmethyl)-3,4-dihydro-2H-pyrido[1,2-a]pyrazine-1,6-dione mono TFA salt (50 mg, 0.125 mmol) in anhydrous methylene chloride (2 mL), pyridine (12 μL, 0.149 mmol) and acetic anhydride (14 μL, 0.149 mmol) were added. The reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated under vacuum, and the residue was purified by prep HPLC (Gilson semi preparative HPLC system using a Waters Nova Pak column [10×40 mm I.D. cartridge, C18, 6 μM pore size) eluting with 95-5% water (0.10% TPA)/acetonitrile (0.10% TFA) gradient at 35 mL/min]. Collection and lyophilization of appropriate fractions provided he title compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517532B2
Source datasetuspto-grants-2009_04
ORD IDord-0243612913a64e52920c71349e9b7b6a
Source noteuspto-grants-2009_04