Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027228Generated: October 30, 2026

N-bromobutanimide → HCID 136377159, compound

https://huagongshe.com/reaction/1027228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 136377150HCID 136377150—
SolventDimethylformamideHCID 6228—
ProductHCID 136377159HCID 13637715929%

Reaction Steps

To a mixture of 7-(benzyloxy)-6-(6-(methyl(2,2,6,6-tetramethylpiperidin-4-yl)amino)pyridazin-3-yl)naphthalen-2-ol (100 mg, 0.201 mmol) in DMF (1 mL) was added N-bromosuccinimide (39.4 mg, 0.221 mmol) at 0° C. The reaction mixture was stirred at RT for 1.5 h, then loaded onto a 2 g SCX column, washed with MeOH, and eluted with 2M NH3 in MeOH. The product-containing fractions were concentrated and the crude material was purified via silica gel flash column chromatography to give the desired product as a brown solid (33.6 mg, 29% yield). MS (M+1)=577.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729263B2
Source datasetuspto-grants-2014_05
ORD IDord-77e2950e662b4edab67e2719cd0d73f0
Source noteuspto-grants-2014_05