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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106440Generated: October 30, 2026

Triethylamine → 1,1-Dimethylethyl 4-[(1,2,3,4,7,8,9,10-octahydro-2,3-dioxopyrido[3,4-f]quinoxaline-9-yl)carbonyl]-1-piperidine carboxylate

https://huagongshe.com/reaction/1106440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
Reactant1,4,7,8,9,10-Hexahydropyrido[3,4-f]quinoxaline-2,3-dioneHCID 21253073—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product1,1-Dimethylethyl 4-[(1,2,3,4,7,8,9,10-octahydro-2,3-dioxopyrido[3,4-f]quinoxaline-9-yl)carbonyl]-1-piperidine carboxylateHCID 2125305573%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of N-Boc-4-piperidinecarboxylic acid (158 mg, 0.69 mmol) and carbonyldiimidazole (119 mg, 0.69 mmol) in tetrahydrofuran (3 mL) under a nitrogen atmosphere was reluxed for 15 min. This solution was then added to suspension of the quinoxalinedione from Example 30 (100 mg, 0.46 mmol) in anhydrous dimethylformamide (3 mL). After stirring for 15 min (nitrogen atmosphere), triethylamine (0.96 mL, 0.69 mmol) was added and the reaction was stirred at 70° C. for 19 h. The mixture was concentrated to dryness and the residue triturated with water and collected by filtration. A beige solid (143 mg, 73% yield) was obtained. mp=283-286° C. CHN calc'd for C22H28N4O5 within ±0.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057313
Source datasetuspto-grants-2000_05
ORD IDord-fd373baad19b406abf169c73783c1ae2
Source noteuspto-grants-2000_05