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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518179Generated: November 3, 2026

Pyridine → HCID 131733359, compound

https://huagongshe.com/reaction/518179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantO-BenzylhydroxylamineHCID 102313—
ReactantHCID 52951036HCID 52951036—
SolventEthanolHCID 702—
ProductHCID 131733359HCID 13173335931.6%

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), NH2OCH2Ph (94 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 cooled down to RT and evaporated under vacuum. The crude residue was triturated with Et2O/H2O 90/10 to give (E)-3-{1′-benzyl-4-benzyloxyimino-spiro[chromane-2,4′-piperidine]-6-yl}-N-hydroxy-acrylamide (55 mg) as a 70/30 mixture of the two isomers (hydrochloride salts).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115148B2
Source datasetuspto-grants-2015_08
ORD IDord-90c5181ec6be47e08bccacd0a3b854f8
Source noteuspto-grants-2015_08