Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518181Generated: November 3, 2026

Pyridine → HCID 86651037, compound

https://huagongshe.com/reaction/518181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 52951036HCID 52951036—
SolventEthanolHCID 702—
ProductHCID 86651037HCID 86651037105.2%

Reaction Steps

A mixture of (E)-3-{1′-Benzyl-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-N-hydroxy-acrylamide hydrochloride (150 mg, 0.35 mmol), NH2OH.HCl (53 mg, 0.76 mmol) and pyridine (61 μl, 0.700 mmol) in EtOH (10 ml) was heated to reflux. After 2 h, the solution was evaporated under vacuum. The crude residue was triturated with Et2O/H2O 90/10 to give (E)-3-{1′-benzyl-4-hydroxyimino-spiro[chromane-2,4′-piperidine]-6-yl}-N-hydroxy-acrylamide (150 mg) as a 98/2 mixture of the two isomers (hydrochloride salts).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115148B2
Source datasetuspto-grants-2015_08
ORD IDord-1ee2fcf6d66a40d5a24b9c6f6919ed87
Source noteuspto-grants-2015_08