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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339012Generated: October 29, 2026

Ethanol → HCID 86707513, compound

https://huagongshe.com/reaction/339012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium BicarbonateHCID 516892—
ReactantAcetic acid;iodosylbenzeneHCID 73357407—
Reactanttert-butyl (S)-1-((R)-2,2,2-trifluoro-1-(6-hydrazinylpyridin-3-yl)ethyl)pyrrolidin-3-ylcarbamateHCID 86707414—
ReactantHCID 86707512HCID 86707512—
SolventEthyl AcetateHCID 8857—
ProductHCID 86707513HCID 8670751349%

Reaction Steps

A solution of tert-butyl (S)-1-((R)-2,2,2-trifluoro-1-(6-hydrazinylpyridin-3-yl)ethyl)pyrrolidin-3-ylcarbamate (0.16 g, 0.39 mmol) and (S)-8-(2-hydroxypropoxy)quinoline-2-carbaldehyde (0.91 g, 0.39 mmol) in ethanol (2.0 mL, 0.39 mmol) was allowed to stir at ambient temperature for 12 hours. The solvent was removed under reduced pressure. The residue was dissolved in dichloromethane (2.0 mL) and iodosobenzene diacetate (0.14 g, 0.43 mmol) was added. The reaction mixture was stirred at ambient temperature for 1 hour. Ethyl acetate (20 mL) and saturated sodium bicarbonate (10 mL) were added. The organic layer was separated, washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by reverse phase chromatography on C18 (0-100% acetonitrile/water) to give the title compound (0.11 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-7d61b566cce343b8a83772dccf8e2906
Source noteuspto-grants-2014_11