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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423887Generated: November 3, 2026

4-Pyridinecarboxaldehyde → HCID 68958548, compound

https://huagongshe.com/reaction/1423887

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinecarboxaldehydeHCID 13389—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Isocyano-1-(4-methylpiperazin-1-yl)ethanoneHCID 181913—
SolventMethanolHCID 887—
ProductHCID 68958548HCID 6895854878%

Reaction Steps

To a stirred and cooled (0° C.) solution of KOH (0.335 g, 5.98 mmol) in 7 mL MeOH were added successively pyridine-4-carbaldehyde (0.705 g, 6.58 mmol) and 2-isocyano-1-(4-methyl-piperazin-1-yl)-ethanone VIB 01128 (1.00 g, 6.58 mmol). The mixture was stirred at 0° C. until precipitation and concentrated. The mixture was partitioned between EtOAc (20 mL) and H2O (10 mL). The aqueous layer was extracted twice with EtOAc (60 mL). The EtOAc fractions were combined, washed twice with brine (2×10 mL), dried over MgSO4 and filtered. After evaporation and drying trans-(4,5-dihydro-5-(pyridin-4-yl)oxazol-4-yl)(4-methylpiperazin-1-yl)methanone VIB 01130 was obtained (1.282 g, 78% yield) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927589B2
Source datasetuspto-grants-2015_01
ORD IDord-368a903ebcaa478dad1110cde2417b3d
Source noteuspto-grants-2015_01