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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654537Generated: October 31, 2026

Pyridine → HCID 131718969, compound

https://huagongshe.com/reaction/1654537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 131718968HCID 131718968—
SolventDimethylformamideHCID 6228—
ProductHCID 131718969HCID 131718969—

Reaction Conditions

Temperature70 °C

Reaction Steps

1-[3-(Indan-2-ylacetyl)-L-thioprolyl]-L-prolinal (1.12 g), hydroxylamine hydrochloride salt (229 mg) and pyridine (266 μl) were dissolved in 10 ml of dimethylformamide, and stirred at 70° C. for 1.5 hours to obtain (2S)-1-[3-(indan-2-ylacetyl)-L-thioprolyl]-2-pyrrolidine aldoxime. Subsequently, 366 mg of selenium dioxide was added to the reaction solution, followed by agitation at 70° C. for 3 hours. The residue of selenium dioxide was filtered under aspiration, and the resulting filtrate was concentrated under reduced pressure. The residue was dissolved in 50 ml of methylene chloride, washed sequentially in 1N hydrochloric acid, saturated aqueous sodium chloride solution, and saturated aqueous sodium chloride solution, and dried over magnesium sulfate, followed by distillation of the solvent under reduced pressure. The resulting residue was purified by column chromatography to obtain 278 mg of (2S)-1-[3-(indan-2-yl-acetyl)-L-thioprolyl]-2-cyanopyrrolidine. Yield; 25%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05407950
Source datasetuspto-grants-1995_04
ORD IDord-361c172cee90406292e7380f6e5b17ba
Source noteuspto-grants-1995_04