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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944002Generated: October 30, 2026

2-Bromo-1-(thiophen-2-yl)ethan-1-one → N-[2-(Thien-2-yl)imidazo[1,2-a]pyrid-7-yl]-5-fluoro-1-[(3-fluorophenyl)methyl]-1H-indole-2-carboxamide

https://huagongshe.com/reaction/1944002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(thiophen-2-yl)ethan-1-oneHCID 2776372—
ReactantN-[2-aminopyrid-4-yl]-5-fluoro-1-[(3-fluorophenyl)methyl]-1H-indole-2-carboxamideHCID 66863747—
SolventAcetonitrileHCID 6342—
ProductN-[2-(Thien-2-yl)imidazo[1,2-a]pyrid-7-yl]-5-fluoro-1-[(3-fluorophenyl)methyl]-1H-indole-2-carboxamideHCID 6686341920.6%

Reaction Steps

Compound 11 was prepared according to a process similar to that described in step 10.2, by reacting 0.1 g (0.26 mmol) of N-[2-aminopyrid-4-yl]-5-fluoro-1-[(3-fluoro-phenyl)methyl]-1H-indole-2-carboxamide, prepared according to the protocol described in step 10.1, with 0.11 g (0.53 mmol) of 2-bromo-1-(thien-2-yl)ethanone in 4 mL of acetonitrile. 0.026 g of the expected product is thus obtained in the form of a beige-coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394820B2
Source datasetuspto-grants-2013_03
ORD IDord-a7883e9ca9f64ef383b26bfc616bde00
Source noteuspto-grants-2013_03