Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718712Generated: November 1, 2026

N-bromobutanimide → (3-Bromo-8-morpholinoimidazo[1,2-b]pyridazin-2-yl)methanol

https://huagongshe.com/reaction/718712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant(8-Morpholinoimidazo[1,2-b]pyridazin-2-yl)methanolHCID 117728752—
SolventAcetonitrileHCID 6342—
Product(3-Bromo-8-morpholinoimidazo[1,2-b]pyridazin-2-yl)methanolHCID 117728706—

Reaction Steps

A solution of compound 5d (40.0 g, 171 mmol) in CH3CN (400 mL) was treated dropwise with a solution of NBS (30.2 g, 170 mmol) in CH3CN (906 mL) at −20° C. After addition, the reaction mixture was stirred for 2 h at room temperature. The reaction was quenched by the addition of 50 mL of saturated Na2S2O3 solution. The solids formed were collected by filtration and washed with diethyl ether to afford compound 83a as a white solid. Mass Spectrum (LCMS, ESI pos.): Calcd. for C11H13BrN4O2: 313.0 (M+H). found: 313.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193736B2
Source datasetuspto-grants-2015_11
ORD IDord-cff34138d71540a6ac2d3c1c8da7bb51
Source noteuspto-grants-2015_11