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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558956Generated: October 29, 2026

Diphosgene → {5-Fluoro-4-[2-methyl-4-(2,3,4,5-tetrahydrobenzo[b]azepine-1-carbonyl)-benzylcarbamoyl]-2-oxo-3,4-dihydro-2H-quinoxalin-1-yl}acetic Acid Tert-Butyl Ester

https://huagongshe.com/reaction/558956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphosgeneHCID 10426—
ReactantDiisopropylethylamineHCID 81531—
Reactant(4-(Aminomethyl)-3-methylphenyl)(2,3,4,5-tetrahydro-1H-benzo[b]azepin-1-yl)methanoneHCID 15896086—
Reactant(5-Fluoro-2-oxo-3,4-dihydro-2H-quinoxalin-1-yl)acetic acid tert-butyl esterHCID 57470781—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product{5-Fluoro-4-[2-methyl-4-(2,3,4,5-tetrahydrobenzo[b]azepine-1-carbonyl)-benzylcarbamoyl]-2-oxo-3,4-dihydro-2H-quinoxalin-1-yl}acetic Acid Tert-Butyl EsterHCID 59807173—

Reaction Steps

To a solution of (5-fluoro-2-oxo-3,4-dihydro-2H-quinoxalin-1-yl)acetic acid tert-butyl ester from Example 7A (84 mg, 0.30 mmol) in toluene (4.0 ml) were added trichloromethyl chloroformate (36 μl, 0.30 mmol), diisopropylethylamine (54 μl, 0.30 mmol) and a spatula full of activated carbon. The mixture was heated at reflux for 2 h, cooled, filtered through Celite®, washed with EtOAc and evaporated in vacuo. The residue was taken up in THF (3.0 ml) and added to a solution of (4-aminomethyl-3-methylphenyl)-(2,3,4,5-tetrahydrobenzo[b]azepin-1-yl)methanone from Example F (85 mg, 0.29 mmol) in THF (3.0 ml) while cooling in an ice/water bath. The mixture was allowed to warm to room temperature, stirred for 1 h and evaporated in vacuo. The residue was purified by flash chromatography on silica (eluant EtOAc:pet. ether 75:25) to afford a white solid; yield 120 mg, 66%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063038B2
Source datasetuspto-grants-2011_11
ORD IDord-fa034ab1458e4a149760f524e94f87fd
Source noteuspto-grants-2011_11