Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084458Generated: October 31, 2026

Pyridine → HCID 16749201, compound

https://huagongshe.com/reaction/2084458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 16749428HCID 16749428—
CatalystZincchlorideHCID 3007855—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 16749201HCID 1674920136.2%

Reaction Steps

A solution of tert-butyl (3R)-3-{[({(Z)-amino[1-(methylsulfonyl)-4-piperidinyl]methylidene}amino)oxy]carbonyl}-6-cyclohexylhexanoate (preparation 42) (1.50 g, 1.83 mmol) in toluene (100 ml) was treated with pyridine (90 μl, 1.83 mmol) and anhydrous ZnCl2 (150 mg, 1.83 mmol) and heated at reflux for 20 hours. The reaction mixture was diluted with EtOAc and washed with H2O, brine and H2O, dried over anhydrous Na2SO4 and filtered. The solvent was removed under reduced pressure. The residue was purified on a silica column eluting with a solvent gradient of cyclohexane:EtOAc (90:10) gradually changing to (50:50). The oil was recrystallised from pentane to afford the title compound as a white solid (320 mg, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716861B2
Source datasetuspto-grants-2004_04
ORD IDord-e9be7da3223844e6962a3975f7354a1f
Source noteuspto-grants-2004_04