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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984639Generated: October 26, 2026

Acetic Acid → HCID 178521486, compound

https://huagongshe.com/reaction/1984639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Hydroxy-1-(piperazin-1-yl)ethan-1-oneHCID 18506884—
Reactant4-[2-(4-Glycoloylpiperazin-1-yl)-6-phenylpyrido[2,3-d]pyrimidin-7-yl]benzaldehydeHCID 57713960—
ReactantHCID 178525658HCID 178525658—
SolventEthyl AcetateHCID 8857—
ProductHCID 178521486HCID 178521486—

Reaction Steps

To a solution of 4-[2-(4-glycoloylpiperazin-1-yl)-6-phenylpyrido[2,3-d]pyrimidin-7-yl]benzaldehyde (8-1) (136 mg, 0.292 mmol, prepared from 6-4 and 2-oxo-2-piperazin-1-ylethanol according to the procedure described for the synthesis of 7-1) in DM (5 mL) was added 2-(5-piperidin-4-yl-4H-1,2,4-triazol-3-yl)pyridine trifluoroacetate (73 mg, 0.32 mmol) followed by Et3N (80 μL, 0.51 mmol), AcOH (91 μL, 1.5 mmol) and sodium triacetoxyborohydride (59 mg, 0.28 mmol). The reaction mixture was allowed to stir for 12 hr then diluted with EtOAc and washed with NaHCO3 (sat.), dried with MgSO4, filtered, and concentrated under reduced pressure. The oily residue was purified by reverse phase HPLC (Acetonitrile/0.1% TFA in water gradient) to afford the title compound. LRMS m/z (M+H) Calcd.: 667.8, found 667.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544677B2
Source datasetuspto-grants-2009_06
ORD IDord-03655898f2924acf9d9bc50f6257038a
Source noteuspto-grants-2009_06