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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513596Generated: October 29, 2026

Methyl iodide → 5-Methyl-5H-6-thia-4,5-diaza-chrysene 6,6-dioxide

https://huagongshe.com/reaction/513596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5H-quinolino[8,7-c][1,2]benzothiazine 6,6-dioxideHCID 659101—
SolventTetrahydrofuranHCID 8028—
Product5-Methyl-5H-6-thia-4,5-diaza-chrysene 6,6-dioxideHCID 6818328852%

Reaction Steps

5H-6-Thia-4,5-diaza-chrysene 6,6-dioxide (Example Compound 2) (50 mg, 0.18 mmol) was added to solution of NaH (60% dispersion in mineral oil; 11 mg, 0.27 mmol) dissolved in dry THF (3 ml), under argon, at 0° C., and the mixture was stirred for 15 min. Methyliodide (29 mg, 0.22 mmol) was added and the reaction was allowed to warm to room temperature and stirring continued for 12 h. After completion of the reaction (monitored by TLC), the solvent was removed in vacuo. The residue was dissolved in EtOAc, washed with water and brine. The organic phase was dried (Na2SO4) and concentrated in vacuo. The crude residue was purified by column chromatography with n-hexane/EtOAc (3:1) as the eluent to give the title compound (27 mg, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102688B2
Source datasetuspto-grants-2015_08
ORD IDord-7b4380312f4b48d1ab27e331031c4a83
Source noteuspto-grants-2015_08