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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753771Generated: October 28, 2026

Hydrochloric Acid → HCID 71241085, compound

https://huagongshe.com/reaction/1753771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3,5-DimethoxyanilineHCID 66301—
ReactantHCID 71239758HCID 71239758—
SolventIsopropanolHCID 3776—
ProductHCID 71241085HCID 71241085—

Reaction Steps

3-{3-[2-(3,5-Dimethoxy-phenylamino)-oxazol-5-yl]-phenyl}-1H-pyridin-2-one 219 was prepared as for intermediate I-f above from 3-[3-(2-chloro-oxazol-5-yl)-phenyl]-2-methoxy-pyridine VI-c (40 mg, 0.150 mmol) with 3,5-dimethoxyaniline (29 mg, 0.190 mmol) and HCl (2M in ether, 120 μL, 0.23 mmol) in iPrOH (4 mL). The crude reaction mixture was evaporated under reduced pressure and the residue treated with a saturated solution of NaHCO3 and EtOAc. A precipitate formed from the biphasic mixture and was filtered off and dried to give the compound 219 product as a beige solid (19 mg, 33%). 1H NMR (300 MHz, DMSO-d6) δ 11.86 (s, 1H), 10.35 (s, 1H), 7.96 (s, 1H), 7.70 (dd, J=2.0, 6.9 Hz, 1H), 7.60-7.41 (m, 5H), 6.89 (d, J=2.0 Hz, 2H), 6.32 (t, J=6.7 Hz, 1H), 6.13 (s, 1H), 3.73 (s, 6H). ESI+ MS m/z 390 (M+H)+. Retention time=3.45 min (method 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09168245B2
Source datasetuspto-grants-2015_10
ORD IDord-f2009c0eb75a498cbd5ff87c18a671df
Source noteuspto-grants-2015_10