Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54343Generated: October 25, 2026

Stannous chloride dihydrate → 6-Amino-5,7-dichloro-1,4-dihydro-2,3-quinoxalinedione

https://huagongshe.com/reaction/54343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
Reactant6-Nitro-5,7-dichloro-1,4-dihydro-2,3-quinoxalinedioneHCID 19958577—
SolventEthanolHCID 702—
Product6-Amino-5,7-dichloro-1,4-dihydro-2,3-quinoxalinedioneHCID 2118995344.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred mixture of 6-nitro-5,7-dichloro-1,4-dihydro-2,3-quinoxalinedione (81 mg, 0.295 mMol) in ethanol (3 mL) was added SnCl2.2H2O (331 mg, 1.47 mMol) in one portion. The mixture was refluxed at 80° C. (oil bath 90° C.) with stirring to 0.5 h, to form a clear solution and continually refluxed for another 0.5 h. It was then cooled to room temperature and the yellow precipitate was collected by filtration, followed by washing with cold ethanol (2×1 mL) to give 70 mg (97%) of crude title compound (contains minor impurities by NMR). Crystallization from DMSO/H2O gave 32 mg of pure title compound as bright yellow needles; mp: 342°-5° C. (dec. from 335° C.), changed color from 325° C. IR (KBr, cm-1): 3468, 3362, 3193, 1693, 1631, 1493, 1375; NMR (1H, DMSO-d6): δ5.418 (s, 2H); 6.999 (s, 1H); 11.238 (s, 1H); 11.776 (s, 1H). HRMS: calcd for C8H5N3O2Cl2 (M+) m/z: 244.9757; found 244.9769. Potency relative to DCK: 8.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622952
Source datasetuspto-grants-1997_04
ORD IDord-b5c63af961c5446f91566fe19904477f
Source noteuspto-grants-1997_04