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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847090Generated: November 2, 2026

Acetic Acid → 6-[(4R)-4-{[3-(7-Fluoro-2-oxoquinoxalin-1(2H)-yl)propyl]amino}-2-oxopyrrolidin-1-yl]-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one

https://huagongshe.com/reaction/1847090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl [(3R)-5-oxopyrrolidin-3-yl]carbamateHCID 71301758—
Reactant6-[(4R)-4-amino-2-oxopyrrolidin-1-yl]-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-oneHCID 86724991—
Reactant3-(7-Fluoro-2-oxoquinoxalin-1(2H)-yl)propanalHCID 86725013—
SolventDimethylformamideHCID 6228—
Product6-[(4R)-4-{[3-(7-Fluoro-2-oxoquinoxalin-1(2H)-yl)propyl]amino}-2-oxopyrrolidin-1-yl]-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-oneHCID 8672501429%

Reaction Steps

Acetic acid (0.042 ml, 0.70 mmol) was added to a mixture of 3-(7-fluoro-2-oxoquinoxalin-1(2H)-yl)propanal (0.120 g, 0.54 mmol), 6-[(4R)-4-amino-2-oxopyrrolidin-1-yl]-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one (synthesized using [(3R)-5-oxopyrrolidin-3-yl]carbamic acid tert-butyl ester synthesized with reference to WO2004/22536 in the same manner as in Reference Examples 20, 21 and 22; 0.185 g, 0.70 mmol) and N,N-dimethylformamide (1.6 ml). The mixture was stirred for 0.5 hours, to which sodium triacetoxyborohydride (0.15 g, 0.70 mmol) was gradually added and stirred for 12 hours. An aqueous solution of sodium hydrogen carbonate was added to the reaction mixture under cooling on ice and the mixture was extracted with ethyl acetate. The obtained crude product was purified by thin layer chromatography (dichloromethane/methanol) to yield 70 mg (29%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952010B2
Source datasetuspto-grants-2015_02
ORD IDord-293ae2fb844341899a990d057b13e099
Source noteuspto-grants-2015_02