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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279266Generated: November 1, 2026

Pyridine → 2-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-6,7-dihydro-5H-quinolin-8-one oxime

https://huagongshe.com/reaction/2279266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant2-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-6,7-dihydro-5H-quinolin-8-oneHCID 118081839—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-6,7-dihydro-5H-quinolin-8-one oximeHCID 13724005658%

Reaction Steps

A solution of 2-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-6,7-dihydro-5H-quinolin-8-one (0.024 g, 0.067 mmol) was dissolved in ethanol (1 mL) and pyridine (0.054 mL, 0.053 g, 0.67 mmol) was added at ambient temperature. To this was added H2N—OH.HCl (0.0070 g, 0.10 mmol) and the resulting yellowish suspension was stirred at ambient temperature monitoring by LCMS. The reaction was complete after 2 hours. The reaction mixture was diluted with water and extracted ethyl acetate. The organic phase was then washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography eluting with a 5 to 10% MeOH: CH2Cl2, gradient gave 13 mg (58%) of the title compound as a yellow solid, and as a single isomer with mp=212-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133218B2
Source datasetuspto-grants-2015_09
ORD IDord-e7c6123a450f41279c76f8ff17dfc05c
Source noteuspto-grants-2015_09