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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944015Generated: October 31, 2026

Ethyl bromopyruvate → N-[2-(Ethyloxycarbonyl)imidazo[1,2-a]pyrid-6-yl]-5-fluoro-1-[(3-fluorophenyl)methyl]-1H-indole-2-carboxamide

https://huagongshe.com/reaction/1944015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantN-[6-aminopyrid-3-yl]-5-fluoro-1-[(3-fluorophenyl)methyl]-1H-indole-2-carboxamideHCID 66863527—
SolventAcetonitrileHCID 6342—
ProductN-[2-(Ethyloxycarbonyl)imidazo[1,2-a]pyrid-6-yl]-5-fluoro-1-[(3-fluorophenyl)methyl]-1H-indole-2-carboxamideHCID 6686404240.5%

Reaction Steps

Compound 22 was prepared according to a process similar to that described in step 4.3, by reacting 0.1 g (0.26 mmol) of N-[6-aminopyrid-3-yl]-5-fluoro-1-[(3-fluorophenyl)-methyl]-1H-indole-2-carboxamide, prepared according to the protocol described in step 4.2, with 0.105 g (0.53 mmol) of ethyl 3-bromo-2-oxopropionate in 4 mL of acetonitrile. 0.05 g of the expected product is obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394820B2
Source datasetuspto-grants-2013_03
ORD IDord-398e1f29b4504e9bb611c21e11ccc169
Source noteuspto-grants-2013_03