Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025481Generated: October 25, 2026

Water → (1-Bromo-imidazo[1,2-a]quinoxalin-4-yl)isobutyl-amine

https://huagongshe.com/reaction/1025481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsobutylamineHCID 6558—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Bromo-4-chloroimidazo[1,2-A]quinoxalineHCID 71741639—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product(1-Bromo-imidazo[1,2-a]quinoxalin-4-yl)isobutyl-amineHCID 6660158093.3%

Reaction Conditions

Temperature170 °C

Reaction Steps

To a stirred solution of 1-bromo-4-chloro-imidazo[1,2-a]quinoxaline (14.13 g, 50 mmol) in NMP (400 mL) was added isobutylamine (9.94 mL, 100 mmol) and DIPEA (26.13 mL, 150 mmol) at room temperature in a microwave reactor. The solution was heated at 170° C. under microwave irradiation for 60 min. After cooling, water was added to the solution and the precipitate was filtered and the residue was washed with water and dried to give (1-bromo-imidazo[1,2-a]quinoxalin-4-yl)-isobutyl-amine (14.89 g, 93.3%): 1H-NMR (300 MHz, d6-DMSO): δ=9.17 (1H, d), 8.01 (1H, d), 7.92 (1H, s), 7.78 (1H, dd), 7.70 (1H, dd) ppm. UPLC-MS: RT=1.14 min; m/z 284.6 [MH+]; required MW=283.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729082B2
Source datasetuspto-grants-2014_05
ORD IDord-993f3a2439ee4c5ab1082183036ae4d3
Source noteuspto-grants-2014_05