Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582871Generated: October 31, 2026

Water → 2,3-Dimethoxy-8,9-methylenedioxy-dibenzo[c,h]cinnoline

https://huagongshe.com/reaction/1582871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant6-(2-Amino-4,5-methylenedioxyphenyl)-2,3-dimethoxy-naphthaleneHCID 22716437—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
Product2,3-Dimethoxy-8,9-methylenedioxy-dibenzo[c,h]cinnolineHCID 990570750%

Reaction Steps

6-(2-Amino-4,5-methylenedioxyphenyl)-2,3-dimethoxy-naphthalene (13, 40 mg, 0.13 mmol) in acetic acid (2 mL) and concentrated hydrochloric acid (0.3 mL) was cooled to 0° C. and diazotised with a solution of sodium nitrite (0.09 g in 1.5 mL water). The diazonium solution was allowed to rise slowly to room temperature and left overnight. Water (50 mL) was added to the red solution with some precipitate. The resulting mixture was extracted with ethyl acetate, washed with diluted sodium hydroxide solution, then with water, dried (anhydrous Na2SO4) and rotaevaporated to give the crude product. Chromatography on silica gel using 40:60 hexanes:ethyl acetate afforded the title compound (20 mg) in 50% yield; 1H NMR (CDCl3) d 4.09(3H, s), 4.22(3H, s), 6.24(2H, s), 7.31(1H, s), 7.80(1H s), 7.95(1H, s), 8.00(1H, d, J=9.2), 8.13(1H, d, J=8.9), 9.14(1H, s); 13C NMR d 56.5 56.9, 98.1, 102.9, 104.6, 107.5, 107.9, 117.1, 119.6, 120.6, 126.8, 128.5, 131.7, 141.9, 145.6, 150.2, 151.2, 152.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06740650B2
Source datasetuspto-grants-2004_05
ORD IDord-fec3dca9695c4b5bb0a64db93ce728f7
Source noteuspto-grants-2004_05