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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388088Generated: October 27, 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/388088

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 numberUS08372976B2
Source datasetuspto-grants-2013_02
ORD IDord-28929697d25242f9a895cf667eabe9e4
Source noteuspto-grants-2013_02