HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948113Generated: October 25, 2026
Sodium Carbonate → Ethyl 4-(3-methyl-5-nitro-4-oxo-1,4-dihydroquinolin-8-yl)cyclohex-3-ene-1-carboxylate
https://huagongshe.com/reaction/1948113
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(4,4,5,5-Tetramethyl-(1,3,2)dioxaborolan-2-yl)cyclohex-3-ene-1-carboxylic acid ethyl ester | HCID 59278796 | — |
| Reactant | 8-bromo-3-methyl-5-nitroquinolin-4(1H)-one | HCID 67254315 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | Ethyl 4-(3-methyl-5-nitro-4-oxo-1,4-dihydroquinolin-8-yl)cyclohex-3-ene-1-carboxylate | HCID 67254537 | 67% |
Reaction Steps
A mixture of 8-bromo-3-methyl-5-nitroquinolin-4(1H)-one (Compound 304E, 700 mg, 2.47 mmol), ethyl 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)cyclohex-3-enecarboxylate (1.8 g, 6.43 mmol, commercially available or can be prepared according to WO2008/099221), Pd(PPh3)4 (20 mg), and Na2CO3 (1 g, 9.43 mmol) in 1,4-dioxane/H2O (150 mL, 4:1) was evacuated and purged with N2. The reaction mixture was stirred at 100° C. for 18 h under N2. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The material was purified by flash column chromatography to afford the desired compound (600 mg, yield: 67%). 1H NMR (DMSO-d6, 400 MHz): δ=1.22 (t, J=7.2 Hz, 3H), 1.85 (m, 1H), 1.96 (s, 3H), 2.08 (m, 1H), 2.26 (m, 1H), 2.38-2.49 (m, 3H), 2.78 (m, 1H), 4.12 (q, J=7.2 Hz, 2H), 5.84 (s, 1H), 7.46 (d, J=8.0 Hz, 1H), 7.58 (d, J=8.0 Hz, 1H), 7.83 (d, J=6.0 Hz, 1H), 10.94 (d, J=6.0 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399433B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-e74e190ebf334ffc950ee25c3139e633 |
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| Source note | uspto-grants-2013_03 |
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