HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065838Generated: October 31, 2026
Potassium Hydroxide → HCID 68953661, compound
https://huagongshe.com/reaction/2065838
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Bromopyridine-4-carboxaldehyde | HCID 2762997 | — |
| Reactant | Pyrrolidine, 1-(isocyanoacetyl)- | HCID 6455476 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68953661 | HCID 68953661 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288556B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-2870835ad8cc4ed4b0b893d029b415df |
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| Source note | uspto-grants-2012_10 |
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