Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027229Generated: October 28, 2026

Chlorosuccinimide → HCID 136377160, compound

https://huagongshe.com/reaction/1027229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 136377150HCID 136377150—
SolventDimethylformamideHCID 6228—
ProductHCID 136377160HCID 136377160—

Reaction Steps

To a reaction 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 (2 mL) was added N-chlorosuccinimide (32.3 mg, 0.242 mmol) at room temperature. The reaction mixture was stirred overnight then loaded onto an SCX column, washed with MeOH, and eluted with 2 M NH3 in MeOH. The product-containing fractions were concentrated and purified via silica gel flash column chromatography to give the title compound as a light brown solid product (25 mg, 23% yield). MS (M+1)=531.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729263B2
Source datasetuspto-grants-2014_05
ORD IDord-87a786dbf7624432aaabffac0d0f864d
Source noteuspto-grants-2014_05