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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372141Generated: October 31, 2026

Pyridine → HCID 136334154, compound

https://huagongshe.com/reaction/1372141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 21071779HCID 21071779—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 136334154HCID 13633415467%

Reaction Steps

A mixture of 4-(3-fluoro-4-hydroxyphenyl)-naphthalene-1-carbaldehyde (570 mg, 2.13 mmol), hydroxylamine hydrochloride (297 mg, 4.27 mmol), and anhydrous pyridine (0.35 ml, 4.27 mmol) in MeOH (13 ml) was heated to reflux for 1.5 h. The mixture was then diluted with ether, washed with water, the organic layer was dried over anhydrous Na2SO4, passed through a silica plug and concentrated. Purification by reverse phase HPLC (water-CH3CN-0.1% TFA) afforded 400 mg (67%) of product as a white solid: mp 187–188° C.; 1H NMR (300 MHz, DMSO-d6): δ 7.12 (2H, m), 7.28 (1H, d, J=11.4 Hz), 7.45 (1H, d, J=7.4 Hz), 7.53–7.64 (2H, m). 7.83 (1H, d, J=7.5 Hz), 7.90 (1H, d, J=7.6), 8.73 (1H, d, J=8.1 Hz), 8.81 (1H, s), 10.08 (1H, s), 11.46 (1H, s); MS m/z 282 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157491B2
Source datasetuspto-grants-2007_01
ORD IDord-5da5bd5cb81e4400bf50560aa3a12891
Source noteuspto-grants-2007_01