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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040486Generated: October 30, 2026

Methyl iodide → 8-Methoxy-11-methyl-6,11-dihydro-5-thia-4,11-diaza-benzo[a]fluorene

https://huagongshe.com/reaction/2040486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 10778313HCID 10778313—
SolventDimethylformamideHCID 6228—
Product8-Methoxy-11-methyl-6,11-dihydro-5-thia-4,11-diaza-benzo[a]fluoreneHCID 59676078—

Reaction Steps

NaH (60%, 41 mg, 1.03 mmoL) was added into 8-methoxy-6,11-dihydro-5-thia-4,11-diaza-benzo[a]fluorene (250 mg, 0.933 mmoL) in DMF (3 mL) at 0° C. After 10 minutes, MeI (0.064 mL, 0.93 mmoL) was added dropwise into the reaction at 0° C. The reaction mixture was slowly warmed to room temperature over 2 hours. The reaction mixture was then partitioned between EtOAc and saturated NH4Cl. The aqueous phase was extracted two times with EtOAc. The organic layer from each extraction was combined, washed with water, brine, dried over anhydrous Na2SO4, filtered and concentrated to yield a brown oil. The crude material (the oil) was then purified by column chromatography (silica gel, hexanes:EtOAc 1:1 as eluent) to yield the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580840B2
Source datasetuspto-grants-2013_11
ORD IDord-cdbf9c3c7a8f45ac925bdca1a6338f45
Source noteuspto-grants-2013_11