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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189170Generated: October 29, 2026

Hydrochloric Acid → HCID 59363796, compound

https://huagongshe.com/reaction/2189170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2-BENZOTRIAZOL-1-YL-ACETAMIDEHCID 2308125—
ReactantHCID 59363799HCID 59363799—
SolventEthanolHCID 702—
ProductHCID 59363796HCID 5936379639%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of (E)-2-fluoro-5-(3-(2-isobutoxyphenyl)-3-oxoprop-1-enyl)benzonitrile (324 mg, 1 mmol), commercially available 2-(1H-benzo[d][1,2,3]triazol-1-yl)acetamide (176 mg, 1 mmol), and NaOH (80 mg) in 5 mL of EtOH was heated to 50° C. for 5 h. The reaction mixture was acidified with conc. HCl, concentrated and purified by preparative HPLC (reverse-phase, acetonitrile/water with 0.01% ammonium acetate) to afford 2-fluoro-5-(6-{2-[(2-methylpropyl)oxy]phenyl}-2-oxo-1,2-dihydropyridin-4-yl)benzonitrile (70 mg, 39%). 1H NMR (400 MHz, CDCl3): δ 7.90-7.80 (m, 2H), 7.78 (d, 1H), 7.46-7.33 (m, 2H), 7.13-7.03 (m, 2H), 6.62 (d, 2H), 3.85 (d, 2H), 2.21-2.14 (m, 1H), 1.06 (d, 6H). MS (EI) for C22H19FN2O2: 363 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324231B2
Source datasetuspto-grants-2012_12
ORD IDord-cdf5703e74a645da83c934371298ef9b
Source noteuspto-grants-2012_12