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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023163Generated: November 4, 2026

3,4-Dichlorobenzoic acid → HCID 71541849, compound

https://huagongshe.com/reaction/1023163

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzoic acidHCID 5817—
ReactantTriethylamineHCID 8471—
ReactantPropylphosphoric anhydrideHCID 16167369—
ReactantHCID 86680404HCID 86680404—
SolventDimethylformamideHCID 6228—
ProductHCID 71541849HCID 715418494.81%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 2-((2-oxo-1,2-dihydroquinolin-6-yl)oxy)acetohydrazide (0.2 g, 0.858 mmol) and 3,4-dichlorobenzoic acid (0.163 g, 0.858 mmol)) in DMF (8 mL) was added triethylamine (0.598 mL, 4.29 mmol) and propylphosphonic anhydride (T3P) (0.819 g, 2.57 mmol). The reaction mixture was heated at 100° C. overnight under N2 atm. The reaction mixture was concentrated to remove solvent and ice-cold water was added. The precipitate was filtered and washed with water to afford a brown solid. The crude product was purified by preparative HPLC on a C18 reverse phase column (ACN-NH4OAc method) to give 6-((5-(3,4-dichlorophenyl)-1,3,4-oxadiazol-2-yl)methoxy)quinolin-2(1H)-one as a white solid (0.016 g, 4.81%). 1H NMR: 400 MHZ, DMSO-d6: δ 5.51 (s, 1H), 6.52 (d, J=9.60 Hz, 1H), 7.27-7.31 (m, 2H), 7.43 (d, J=2.40 Hz, 1H), 7.83-7.92 (m, 2H), 8.00 (dd, J=1.60, 8.40 Hz, 1H), 8.21 (d, J=1.60 Hz, 1H), 11.68 (s, 1H). LCMS: RT 1.92 min. LCMS (ES-API), m/z 390.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722670B2
Source datasetuspto-grants-2014_05
ORD IDord-20e63d7f0e754c8198839da486bc0165
Source noteuspto-grants-2014_05