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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387205Generated: October 30, 2026

Triethylamine → HCID 18415562, compound

https://huagongshe.com/reaction/1387205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBenzyloxyamine hydrochlorideHCID 102312—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 18415564HCID 18415564—
SolventDimethylformamideHCID 6228—
ProductHCID 18415562HCID 1841556251.5%

Reaction Steps

To an ice-cooled solution of 1-Benzyloxy-7-carboxyquinoxaline-2,3(1H,4H)-dione (422 mg, 1.35 mmol) in 10 ml of N,N-dimethylformamide was added 1-hydroxybenzotriazole (218 mg, 1.48 mmol) followed by 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (272 mg, 1.42 mmol). Stirring was continued for 30 min at 0° C. and O-benzylhydroxylamine hydrochloride (237 mg, 1.49 mmol) and dry triethylamine (0.21 ml, 1.5 mmol) was added. The mixture was stirred overnight at room temperature, then cooled and filtered. The isolated solid was successively washed with water, saturated aqueous sodium hydrogen carbonate and water. Recrystallisation from ethanol gave 290 mg (51%) of the title compound. 1H-NMR (DMSO-d6): 4.95 (s, 2H, CH2), 5.19 (s, 2H, CH2), 7.2-7.8 (m, 13H, ArH), 11.8 (br.s, 1H, exchangeable), 12.3 (br.s, 1H, exchangeable).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268163B1
Source datasetuspto-grants-2001_07
ORD IDord-16296b3ac8e34b1ea6fd78d17834db4b
Source noteuspto-grants-2001_07