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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270317Generated: October 26, 2026

Morpholine → 5,7-Dimethyl-2-[4-(4-morpholinyl)phenyl]-4-(3,4,5-trimethoxyphenoxy)imidazo-[5,1-f][1,2,4]triazine

https://huagongshe.com/reaction/1270317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant2-(4-Bromophenyl)-5,7-dimethyl-4-(3,4,5-trimethoxyphenoxy)imidazo[5,1-f][1,2,4]triazineHCID 12095701—
ReactantSodium t-butoxideHCID 23676156—
SolventTolueneHCID 1140—
Product5,7-Dimethyl-2-[4-(4-morpholinyl)phenyl]-4-(3,4,5-trimethoxyphenoxy)imidazo-[5,1-f][1,2,4]triazineHCID 12096690—

Reaction Conditions

Temperature100 °C

Reaction Steps

28 mg (0.29 mmol) of sodium tert-butoxide are introduced into a second Schlenk tube under argon. Subsequently, 100 mg (0.21 mmol) of 2-(4-bromophenyl)-5,7-dimethyl-4-(3,4,5-trimethoxyphenoxy)imidazo[5,1-f][1,2,4]triazine from Exam-ple 16A, 22 mg (0.25 mmol) of morpholine and 2 ml of anhydrous toluene are added. Solution A is likewise added, and the whole is stirred overnight at 100° C. After cooling, the mixture is then filtered off with suction through a glass frit. The filtrate is concentrated to dryness under reduced pressure and purified by flash chromatography (cyclohexane/ethyl acetate 10:1-4:1-3:2-1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202243B2
Source datasetuspto-grants-2007_04
ORD IDord-6dd3637906c246339276c5d7cf01db7d
Source noteuspto-grants-2007_04