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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944007Generated: October 27, 2026

2-Butanone, 3-bromo- → N-(2,3-Dimethylimidazo[1,2-a]pyrid-7-yl)-5-trifluoromethyl-1-[(3-fluorophenyl)methyl]-1H-pyrrolo[2,3-b]pyridine-2-carboxamide

https://huagongshe.com/reaction/1944007

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butanone, 3-bromo-HCID 13142—
ReactantN-[2-aminopyrid-4-yl]-5-trifluoromethyl-1-[(3-fluorophenyl)methyl]-1H-pyrrolo[2,3-b]pyridine-2-carboxamideHCID 66863300—
SolventAcetonitrileHCID 6342—
ProductN-(2,3-Dimethylimidazo[1,2-a]pyrid-7-yl)-5-trifluoromethyl-1-[(3-fluorophenyl)methyl]-1H-pyrrolo[2,3-b]pyridine-2-carboxamideHCID 6686329633.4%

Reaction Steps

Compound 16 was prepared according to a process similar to that described in step 15.3, by reacting 0.12 g (0.28 mmol) of N-[2-aminopyrid-4-yl]-5-trifluoromethyl-1-[(3-fluorophenyl)methyl]-1H-pyrrolo[2,3-b]pyridine-2-carboxamide, prepared according to the protocol described in step 15.2, with 0.084 g (0.56 mmol) of 3-bromobutan-2-one in 5 mL of acetonitrile. 45 mg of the expected product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394820B2
Source datasetuspto-grants-2013_03
ORD IDord-0105eacd9aa74ed3ac4eed19feae4765
Source noteuspto-grants-2013_03