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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-(4,4,5,5-Tetramethyl-(1,3,2)dioxaborolan-2-yl)cyclohex-3-ene-1-carboxylic acid ethyl esterHCID 59278796—
Reactant8-bromo-3-methyl-5-nitroquinolin-4(1H)-oneHCID 67254315—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductEthyl 4-(3-methyl-5-nitro-4-oxo-1,4-dihydroquinolin-8-yl)cyclohex-3-ene-1-carboxylateHCID 6725453767%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399433B2
Source datasetuspto-grants-2013_03
ORD IDord-e74e190ebf334ffc950ee25c3139e633
Source noteuspto-grants-2013_03