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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056341Generated: November 1, 2026

Potassium Carbonate → Ethyl 4-((tert-butoxycarbonyl)amino)-2-(2-(3-(tert-butylamino)-2-methyl-5-quinoxalinyl)-2-oxoethyl)-4-methyl-3-oxopentanoate

https://huagongshe.com/reaction/1056341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 4-((tert-butoxycarbonyl)amino)-4-methyl-3-oxopentanoateHCID 87815948—
Reactant2-Bromo-1-(3-(tert-butylamino)-2-methylquinoxalin-5-yl)ethanoneHCID 89782142—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-((tert-butoxycarbonyl)amino)-2-(2-(3-(tert-butylamino)-2-methyl-5-quinoxalinyl)-2-oxoethyl)-4-methyl-3-oxopentanoateHCID 8978196932%

Reaction Steps

To a sealable vial was added 2-bromo-1-(3-(tert-butylamino)-2-methylquinoxalin-5-yl)ethanone (606) (1.0 g, 2.97 mmol), ethyl 4-((tert-butoxycarbonyl)amino)-4-methyl-3-oxopentanoate (466a) (0.98 g, 3.57 mmol), DMF (20 mL), and K2CO3 (1.03 g, 7.44 mmol). The solution was stirred at RT for 2 d. The solution was poured into sat NaHCO3 (200 mL) and extracted with EtOAc (3×100 mL). The combined extracts were washed with H2O (3×100 mL), brine (100 mL), dried (Na2SO4) and concentrated onto silica. Purification by silica gel chromatography (0 to 50% EtOAc/hexanes) afforded the title compound as a yellow solid (0.50 g, 0.95 mmol, 32% yield). m/z (ESI, +ve ion) 529.3 (M+H)+. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.87 (dd, J=8.0, 1.6 Hz, 1H), 7.68 (dd, J=7.4, 1.6 Hz, 1H), 7.64 (br. s, 1H), 7.35 (t, J=7.7 Hz, 1H), 6.09 (br. s, 1H), 4.61 (dd, J=10.3, 2.8 Hz, 1H), 4.15 (dd, J=18.5, 10.5 Hz, 1H), 3.98-4.08 (m, 2H), 3.46 (dd, J=18.5, 3.4 Hz, 1H), 2.55 (s, 3H), 1.52 (s, 9H), 1.29 (s, 3H), 1.28 (s, 3H), 1.24 (s, 9H), 1.12 (t, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394297B2
Source datasetuspto-grants-2016_07
ORD IDord-38c7b69c2eb744eda26cd685980d595b
Source noteuspto-grants-2016_07