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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882070Generated: October 27, 2026

4-((6-(Trifluoromethyl)pyridin-3-yl)methoxy)pyridin-2(1H)-one → tert-Butyl 7-(2-oxo-4-((6-(trifluoromethyl)pyridin-3-yl)methoxy)pyridin-1(2H)-yl)-3,4-dihydropyrido[4',3':4,5]imidazo[1,2-a]pyridine-2(1H)-carboxylate

https://huagongshe.com/reaction/882070

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((6-(Trifluoromethyl)pyridin-3-yl)methoxy)pyridin-2(1H)-oneHCID 57950360—
Reactanttert-Butyl 7-bromo-3,4-dihydropyrido[4',3':4,5]imidazo[1,2-a]pyridine-2(1H)-carboxylateHCID 67988849—
Producttert-Butyl 7-(2-oxo-4-((6-(trifluoromethyl)pyridin-3-yl)methoxy)pyridin-1(2H)-yl)-3,4-dihydropyrido[4',3':4,5]imidazo[1,2-a]pyridine-2(1H)-carboxylateHCID 6805612944%

Reaction Steps

tert-Butyl 7-bromo-3,4-dihydropyrido[4′,3′:4,5]imidazo[1,2-a]pyridine-2(1H)-carboxylate (175 mg, 0.498 mmol) and 4-((6-(trifluoromethyl)pyridin-3-yl)methoxy)pyridin-2(1H)-one (134 mg, 0.498 mmol) were reacted according to Example 18 (step g) to provide the title compound (104 mg, 44%) as a yellow solid: ESI MS m/z 542 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993765B2
Source datasetuspto-grants-2015_03
ORD IDord-f4158e8e8446427da830ad08f795738a
Source noteuspto-grants-2015_03