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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242618Generated: October 31, 2026

Carbon Disulfide → tert-butyl (2S,4EZ)-4-(methoxy-imino)-2-(5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-1-pyrrolidinecarboxylate

https://huagongshe.com/reaction/1242618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantPotassium HydroxideHCID 14797—
Reactanttert-butyl (2S,4EZ)-2-(hydrazinocarbonyl)-4-(methoxyimino)-1-pyrrolidinecarboxylateHCID 58714558—
SolventEthanolHCID 702—
Producttert-butyl (2S,4EZ)-4-(methoxy-imino)-2-(5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-1-pyrrolidinecarboxylateHCID 131725971—

Reaction Steps

To a solution of tert-butyl (2S,4EZ)-2-(hydrazinocarbonyl)-4-(methoxyimino)-1-pyrrolidinecarboxylate (Intermediate 9, 2.86 mmoles; 780 mg) in ethanol (25 mL) at 0° C. was added carbon disulfide (6.86 mmoles; 522 mg) and potassium hydroxide (3 mmoles; 168 mg). The mixture was refluxed for 7 h. The solvent was evaporated and the residue re-dissolved in EtOAc and washed with NH4Cl sat and 10% NaHCO3 and brine. The organic layer was dried over Na2SO4 and evaporated to give the desired N-protected intermediate, tert-butyl (2S,4EZ)-4-(methoxyimino)-2-(5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-1-pyrrolidine-carboxylate, as a yellowish oil (200 mg, 23%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115639B2
Source datasetuspto-grants-2006_10
ORD IDord-caac2c05ef024598bc28c95dc461eafa
Source noteuspto-grants-2006_10