Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930053Generated: November 2, 2026

HCID 57929903, compound → HCID 57929880, compound

https://huagongshe.com/reaction/1930053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57929903HCID 57929903—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
ProductHCID 57929880HCID 5792988098%

Reaction Steps

The 6-(1-(2-azidoethyl)-5-(2,4-difluorophenyl)-1H-pyrazol-4-yl)-3-isopropyl-[1,2,4]triazolo[4,3-b]pyridazine (0.485 g, 1.19 mmol; prepared using General Procedure L.1 from 1-(2,4-difluorophenyl)-2-(3-isopropyl-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)ethanone (Preparation #K.1) with hydroxylethylhydrazine, General Procedure W with methanesulfonyl chloride, General Procedure X.1 with sodium azide) was dissolved in EtOH (20 mL) then platinum (IV) oxide (0.090 g, 0.40 mmol) was added. The mixture was hydrogenated at atmospheric pressure and ambient temperature for about 16 h then filtered through a pad of Celite®. The filtrate was concentrated under reduced pressure to give the title compound (0.447 g, 98%): LC/MS (Table 1, Method a) Rt=1.66 min; MS m/z: 384.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188083B2
Source datasetuspto-grants-2012_05
ORD IDord-d49c785eb2ec44c4808e3235e084eb87
Source noteuspto-grants-2012_05