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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014684Generated: October 31, 2026

(3-Amino-6-(5-quinolyl)pyrazin-2-yl)[(4-methoxyphenyl)methyl]amine → 5-(Quinolin-5-YL)-1H-imidazo[4,5-B]pyrazin-2(3H)-one

https://huagongshe.com/reaction/1014684

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Amino-6-(5-quinolyl)pyrazin-2-yl)[(4-methoxyphenyl)methyl]amineHCID 66699817—
Reactant5-(5-Quinolyl)pyrazine-2,3-diamineHCID 66699852—
SolventThiophenolHCID 7969—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Product5-(Quinolin-5-YL)-1H-imidazo[4,5-B]pyrazin-2(3H)-oneHCID 2498467857%

Reaction Conditions

Temperature70 °C

Reaction Steps

5-(5-Quinolyl)pyrazine-2,3-diamine. (3-Amino-6-(5-quinolyl)pyrazin-2-yl)[(4-methoxy phenyl)methyl]amine (see Example 1.B) (0.210 g, 0.588 mmol) was dissolved in trifluoroacetic acid/dichloromethane (2 mL:2 mL) with PS-thiophenol as a scavenger. The solution was heated to 70° C. in a sealed tube for two hours and then concentrated under reduced pressure and diluted with methanol. The methanol/product solution was filtered through a Phenomenex Strata-X-C solid phase extraction column to remove TFA. Additional water was added to the eluted compound to induce precipitation. The precipitate was filtered and dried under vacuum to afford the title compound (0.080 g, 57% yield). MS (ESI) m/z 238.1 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981893B2
Source datasetuspto-grants-2011_07
ORD IDord-ed0fb4b255e74caf912e9fd8124cb7ff
Source noteuspto-grants-2011_07