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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360248Generated: November 1, 2026

Diisopropylethylamine → HCID 66788954, compound

https://huagongshe.com/reaction/1360248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Chloro-2-methoxybenzene-1-sulfonyl chlorideHCID 2734272—
ReactantHCID 66789204HCID 66789204—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 66788954HCID 66788954—

Reaction Steps

3,4-Dihydro-2H-quinoxaline-1,6-dicarboxylic acid 1-tert-butyl ester 6-ethyl ester (300 mg, 0.98 mmol) was dissolved in dichloromethane (20 mL) and pyridine (2 mL). N,N-Diisopropylethylamine (127 mg, 0.98 mmol) and 5-chloro-2-methoxy-benzenesulfonyl chloride (300 mg, 1.24 mmol) were added, and the mixture was stirred at room temperature overnight. The solvent was evaporated, and the crude compound was purified by flash chromatography, yielding 4-(5-chloro-2-methoxy-benzenesulfonyl)-3,4-dihydro-2H-quinoxaline-1,6-dicarboxylic acid 1-tert-butyl ester 6-ethyl ester as a light yellow gum, 435 mg (87%), H (300 MHz; CDCl3) 8.17 (1H, s), 8.05 (1H, s), 7.82 (1H, d), 7.74 (1H, d), 7.46 (1H, dd), 6.82 (1H, d), 4.35 (2H, q), 3.93 (2H, m), 3.71 (2H, m), 3.56 (3H, s), 1.48 (9H, s), 1.39 (3H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879845B2
Source datasetuspto-grants-2011_02
ORD IDord-365a770abbe64dcd99834b2b6f1a87e5
Source noteuspto-grants-2011_02