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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dichlorobenzoic acid | HCID 5817 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propylphosphoric anhydride | HCID 16167369 | — |
| Reactant | HCID 86680404 | HCID 86680404 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 71541849 | HCID 71541849 | 4.81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722670B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-20e63d7f0e754c8198839da486bc0165 |
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| Source note | uspto-grants-2014_05 |
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