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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870721Generated: November 1, 2026

Triethylamine → (3-Bromo-imidazo[1,2-b]pyridazin-6-yl)-[2-(2-ethoxy-phenyl)-ethyl]-amine

https://huagongshe.com/reaction/870721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-EthoxyphenethylamineHCID 142362—
Reactant3-Bromo-6-fluoroimidazo[1,2-b]pyridazineHCID 86696318—
SolventIsopropanolHCID 3776—
Product(3-Bromo-imidazo[1,2-b]pyridazin-6-yl)-[2-(2-ethoxy-phenyl)-ethyl]-amineHCID 8669642690.4%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 3-bromo-6-fluoro-imidazo[1,2-b]pyridazine (648 mg, 3 mmol), 2-ethoxy-phenethylamine (1 g, 6 mmol) and triethylamine (1 ml) in isopropyl alcohol (2 ml) was heated in a microwave at 140° C. for 20 min. The reaction mixture was concentrated and the residue was subjected to ISCO (40 g column), to gave the titled compound (980 mg). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.47 (t, J=6.95 Hz, 3H) 3.04 (t, J=6.69 Hz, 2H) 3.64-3.72 (m, 2H) 4.06-4.17 (m, 2H) 4.97 (br. s., 1H) 6.40 (d, J=9.60 Hz, 1H) 6.87-7.02 (m, 2H) 7.17-7.32 (m, 2H) 7.47 (s, 1H) 7.54 (d, J=9.60 Hz, 1H). LRMS (ESI) m/z 361 and 363.1 [(M+H)]+, calc'd for C16H17BrN4O: 361.24.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969565B2
Source datasetuspto-grants-2015_03
ORD IDord-763a34fd18584837a442444fcfe6f03a
Source noteuspto-grants-2015_03