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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358273Generated: October 25, 2026

N4-(3-bromophenyl)-4,6,7-Quinazolinetriamine → N-(3-bromophenyl)pyrazino[2,3-g]quinazolin-4-amine

https://huagongshe.com/reaction/1358273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN4-(3-bromophenyl)-4,6,7-QuinazolinetriamineHCID 2426—
Reactant1,4-Dioxane-2,3-diolHCID 96170—
SolventMethanolHCID 887—
ProductN-(3-bromophenyl)pyrazino[2,3-g]quinazolin-4-amineHCID 532824684.1%

Reaction Steps

A mixture of 4-(3-bromoanilino)-6,7-diaminoquinazoline (90 mg, 0.27 mmol) and 1,4-dioxane-2,3-diol (0.2 g, 1.6 mmol) [Venuti, M. C.; Synthesis, 1982, 61-63] in MeOH (20 mL) is stirred at room temperature overnight to give a precipitate of 4-(3-bromoanilino)pyrazino[2,3-g]quinazoline (80 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596726B1
Source datasetuspto-grants-2003_07
ORD IDord-9bc38be78ea04612aa042065386db123
Source noteuspto-grants-2003_07