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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007114Generated: October 28, 2026

Toluene → isopropyl 7-bromo-3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate

https://huagongshe.com/reaction/1007114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantIsopropyl chloroformateHCID 7917—
Reactant6-Bromo-1,2-dihydroquinoxalin-2-oneHCID 12686394—
SolventPyridineHCID 1049—
Productisopropyl 7-bromo-3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylateHCID 1846440597%

Reaction Steps

To a solution of 7-bromo-3-oxo-3,4-dihydroquinoxaline (6.8 g, 30 mmol) in pyridine (50 ml) was added a solution of isopropyl chloroformate in toluene (35 ml, 1M, 35 mmol) over 30 minutes. The mixture was triturated with water/chloroform, the organic layer was separated, washed with brine, dried over magnesium sulfate, and evaporated to obtain crude isopropyl 7-bromo-3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate(9.3 g, 97%). A sample was recrystallized from ethanol: m.p. 159-161° C. 1H-NMR (DMSO-d6) δ 1.25 (d, J=6.2 Hz, 6H), 4.25 (s, 2H), 4.90 (Sep, J=6.2 Hz, 1H), 6.89 (d, J=8.6 Hz, 1H), 7.27 (dd, J=9.1, 2.1 Hz, 1H), 7.74 (s, 1H), 12.51 (s, 1H), MS (ESI) m/z 330/332 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794373B2
Source datasetuspto-grants-2004_09
ORD IDord-605b71f5872e4b45a9bc43b1a0dfaa1d
Source noteuspto-grants-2004_09