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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845892Generated: October 30, 2026

3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1-(1-(diphenylmethyl)azetidin-3-yl)-1H-1,2,3-triazol-4-yl)-2-aminopyridine → 3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1-(azetidin-3-yl)-1H-1,2,3-triazol-4-yl)-2-aminopyridine

https://huagongshe.com/reaction/1845892

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1-(1-(diphenylmethyl)azetidin-3-yl)-1H-1,2,3-triazol-4-yl)-2-aminopyridineHCID 89708470—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1-(azetidin-3-yl)-1H-1,2,3-triazol-4-yl)-2-aminopyridineHCID 89708474—

Reaction Steps

The product of the above mentioned Example 9 3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1-(1-(diphenylmethyl)azetidin-3-yl)-1H-1,2,3-triazol-4-yl)-2-aminopyridine (2.2 g, 3.73 mmol) was dissolved in methanol (40 mL), and palladium hydroxide/carbon (220 mg) was added to perform the hydrogenation reaction. TLC test showed that the raw materials were completely reacted. After filtration, the filtrate was concentrated under reduced pressure to yield the target product as white solid powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952002B2
Source datasetuspto-grants-2015_02
ORD IDord-7b71a70d925c49998cc7943a045704c8
Source noteuspto-grants-2015_02