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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019556Generated: October 30, 2026

2-(3-Azabicyclo[3.1.0]hex-3-yl)-5-aminopyridine → N-[6-(3-Azabicyclo[3.1.0]hex-3-yl)-pyridin-3-yl]-5-fluoro-1-(3-fluorobenzyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxamide

https://huagongshe.com/reaction/1019556

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Azabicyclo[3.1.0]hex-3-yl)-5-aminopyridineHCID 57431531—
Reactant5-Fluoro-1-(3-fluorobenzyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acidHCID 66907943—
ProductN-[6-(3-Azabicyclo[3.1.0]hex-3-yl)-pyridin-3-yl]-5-fluoro-1-(3-fluorobenzyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxamideHCID 6690800367.6%

Reaction Steps

According to a method similar to that described in Stage 12.3, starting from 0.45 g (1.56 mmol) of 5-fluoro-1-[(3-fluorophenyl)methyl]-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, described in the preceding stage, and 0.3 g (1.71 mmol) of 6-(3-azabicyclo[3.1.0]hex-3-yl)-3-aminopyridine, prepared in Stage 21.2, we obtain 0.47 g of the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716272B2
Source datasetuspto-grants-2014_05
ORD IDord-4d1b00bcafad41c4824242e4ccae64df
Source noteuspto-grants-2014_05