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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041943Generated: November 4, 2026

5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acid → N-[6-(3-Hydroxyazetidin-1-yl)pyridin-3-yl]-5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/2041943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acidHCID 57431513—
Reactant1-(5-Aminopyridin-2-yl)azetidin-3-olHCID 57431525—
ProductN-[6-(3-Hydroxyazetidin-1-yl)pyridin-3-yl]-5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamideHCID 57431524—

Reaction Steps

The process is carried out according to the method described in example 2, using 0.5 g (1.74 mmol) of 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acid (example 1.1) and 0.35 g (2.09 mmol) of 2-(3-hydroxyazetidin-1-yl)-5-aminopyridine, obtained in step 10.2 (Compound Ve).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586573B2
Source datasetuspto-grants-2013_11
ORD IDord-320096c8d5934cf99de11bdee57e6ec2
Source noteuspto-grants-2013_11