HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642787Generated: October 30, 2026
Methyl iodide → 8-Methoxy-11-methyl-6,11-dihydro-5-thia-4,11-diaza-benzo[a]fluorene
https://huagongshe.com/reaction/642787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 10778313 | HCID 10778313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-Methoxy-11-methyl-6,11-dihydro-5-thia-4,11-diaza-benzo[a]fluorene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07696239B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-0583ed0e9cd64d0b83ccde003cfc8fae |
|---|
| Source note | uspto-grants-2010_04 |
|---|