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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640477Generated: October 30, 2026

N-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-iodo-4-methylbenzamide → N-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-(imidazo[1,2-a]pyridin-3-ylethynyl)-4-methylbenzamide

https://huagongshe.com/reaction/1640477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-iodo-4-methylbenzamideHCID 44222638—
Reactant3-Ethynylimidazo[1,2-a]pyridineHCID 46838759—
ProductN-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-(imidazo[1,2-a]pyridin-3-ylethynyl)-4-methylbenzamideHCID 24826632—

Reaction Steps

The titled compound was made as for example 1 using N-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-iodo-4-methylbenzamide and 3-ethynylimidazo[1,2-a]pyridine: MS (M+H)+ 486. The titled compound can also be prepared according to the alternative synthesis described in example 1 from 3-(imidazo[1,2-a]pyridin-3-ylethynyl)-4-methylbenzoic acid and 3-(1H-imidazol-1-yl)-5-(trifluoromethyl)aniline (as prepared in Example 1). The 3-(imidazo[1,2-a]pyridin-3-ylethynyl)-4-methylbenzoic acid is prepared in a manner similar to that described in Example 1 using 3-Ethynylimidazo[1,2-a]pyridine and 3-iodo-4-methylbenzoic acid as Sonogashira coupling partners.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114874B2
Source datasetuspto-grants-2012_02
ORD IDord-f4917bdbd45a4da6ab2f8adcf440f1e1
Source noteuspto-grants-2012_02