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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065838Generated: October 31, 2026

Potassium Hydroxide → HCID 68953661, compound

https://huagongshe.com/reaction/2065838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant3-Bromopyridine-4-carboxaldehydeHCID 2762997—
ReactantPyrrolidine, 1-(isocyanoacetyl)-HCID 6455476—
SolventMethanolHCID 887—
ProductHCID 68953661HCID 68953661—

Reaction Conditions

Temperature0 °C

Reaction Steps

BAL 01028A was prepared in accordance with method D using 3-bromo-4-pyridinecarboxaldehyde (1.010 g, 5.43 mmol), KOH (0.305 g, 5.43 mmol) in methanol (5 mL) and 2-isocyano-1-pyrrolidin-1-yl-ethanone BLE 04134 (0.75 g, 5.43 mmol). The mixture was stirred at 0° C. until precipitation and concentrated. The mixture was partitioned between EtOAc (50 ml) and H2O (25 ml). The aqueous layer was extracted twice with EtOAc (25 mL). The EtOAc fractions were combined, washed twice with brine (2×25 mL), dried over MgSO4 and filtered. After evaporation and trans-(5-(3-bromopyridin-4-yl)-4,5-dihydrooxazol-4-yl)(pyrrolidin-1-yl)methanone BAL 01028A was obtained (1.20 g, 68% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288556B2
Source datasetuspto-grants-2012_10
ORD IDord-2870835ad8cc4ed4b0b893d029b415df
Source noteuspto-grants-2012_10