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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056498Generated: November 1, 2026

4-Pyridinecarboxaldehyde → Trans-(4,5-dihydro-5-(pyridin-4-yl)oxazol-4-yl)(pyrrolidin-1-yl)methanone

https://huagongshe.com/reaction/1056498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinecarboxaldehydeHCID 13389—
ReactantPotassium HydroxideHCID 14797—
ReactantPyrrolidine, 1-(isocyanoacetyl)-HCID 6455476—
SolventMethanolHCID 887—
ProductTrans-(4,5-dihydro-5-(pyridin-4-yl)oxazol-4-yl)(pyrrolidin-1-yl)methanoneHCID 6690153898%

Reaction Steps

Compound 19 was prepared in accordance with method D using pyridine-4-carbaldehyde (1.88 mL, 19.76 mmol), KOH (1.01 g, 18.00 mmol) in methanol (18 mL) and 2-isocyano-1-(pyrrolidin-1-yl)ethanone BLE 04098 (2.73 g, 19.76 mmol). The residue was partitioned between ethyl acetate (200 mL) and water (150 mL). The organic layer was combined with additional ethyl acetate extracts (2×150 mL), washed with aqueous sodium chloride (2×150 mL) and dried over MgSO4, filtered and evaporated. Trans-(4,5-dihydro-5-(pyridin-4-yl)oxazol-4-yl)(pyrrolidin-1-yl)methanone Compound 19 was obtained as a white solid (4.32 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399628B2
Source datasetuspto-grants-2016_07
ORD IDord-2bbb806379c442cba1c9ac3d0263ec54
Source noteuspto-grants-2016_07