Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176157Generated: November 1, 2026

Butanedione → 4,9-Dibromo-6,7-dimethyl-[1,2,5]thiadiazolo[3,4-g]quinoxaline

https://huagongshe.com/reaction/1176157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanedioneHCID 650—
ReactantWaterHCID 962—
Reactant4,7-Dibromo-2,1,3-benzothiadiazole-5,6-diamineHCID 68408343—
SolventAcetic AcidHCID 176—
Product4,9-Dibromo-6,7-dimethyl-[1,2,5]thiadiazolo[3,4-g]quinoxalineHCID 68408344—

Reaction Steps

5,6-Diamino-4,7-dibromobenzo[c][1,2,5]thiadiazole (0.257 g, 7.93×10−4 mol) was dissolved in acetic acid (30 ml). 2,3-Butanedione (0.30 ml, 3.4×10−3 mol) was added, and the reaction mixture was stirred for 19 h at room temperature under N2. Water (50 ml) was added, and the resulting precipitate was filtered, dissolved in CH2Cl2, washed with water, and dried over Na2SO4. After the solvent was evaporated, the residue was chromatographed on silica gel with CHCl3. Yield=0.256 g (86% based on 0.257 g of 5,6-diamino-4,7-dibromobenzo[c][1,2,5]thiadiazole). 1H NMR (360 MHz, CDCl3): δ 2.88 (s, 6H, —CH3). Chemical Ionization MS m/z: 371.8675 (M+) (calcd 371.868).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842758B2
Source datasetuspto-grants-2010_11
ORD IDord-85717c072ea944ec9c9f57e780545a43
Source noteuspto-grants-2010_11