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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423882Generated: November 2, 2026

Potassium Hydroxide → HCID 68953661, compound

https://huagongshe.com/reaction/1423882

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 numberUS08927589B2
Source datasetuspto-grants-2015_01
ORD IDord-178a6727b90c48f2a1070d2ae00de680
Source noteuspto-grants-2015_01