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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171402Generated: October 30, 2026

(4-((6-Chloropyridin-3-yl)oxy)-3-fluorophenyl)methanol → 7-((4-((6-chloropyridin-3-yl)oxy)-3-fluorobenzyl)oxy)-2,2-dimethyl-2,3-dihydroimidazo[1,2-c]pyrimidin-5(1H)-one

https://huagongshe.com/reaction/2171402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-((6-Chloropyridin-3-yl)oxy)-3-fluorophenyl)methanolHCID 86676396—
Reactanttert-butyl 7-chloro-2,2-dimethyl-5-oxo-2,3-dihydroimidazo[1,2-c]pyrimidine-1(5H)-carboxylateHCID 86728374—
Product7-((4-((6-chloropyridin-3-yl)oxy)-3-fluorobenzyl)oxy)-2,2-dimethyl-2,3-dihydroimidazo[1,2-c]pyrimidin-5(1H)-oneHCID 86728382—

Reaction Steps

The title compound was prepared by a procedure similar to that described for E9 starting from (4-((6-chloropyridin-3-yl)oxy)-3-fluorophenyl)methanol and tert-butyl 7-chloro-2,2-dimethyl-5-oxo-2,3-dihydroimidazo[1,2-c]pyrimidine-1(5H)-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051325B2
Source datasetuspto-grants-2015_06
ORD IDord-f0839fcc32834d9ba46f1a0071e84414
Source noteuspto-grants-2015_06