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CAS No. : | 41532-84-7 | MDL No. : | MFCD00082627 |
Formula : | C15H15N | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | WJZSZXCWMATYFX-UHFFFAOYSA-N |
M.W : | 209.29 | Pubchem ID : | 170530 |
Synonyms : |
|
Chemical Name : | 1,1,2-Trimethyl-1H-benzo[e]indole |
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With acetic acid; at 100℃; for 24h; | General procedure: In parallel, substituted hydrazines 1 (4.0 g, 22.25 mmol) were reacted with 3-methylbutanone(3 mL, 28.04 mmol) in acetic acid and heated to a 100 C for 24 h. The solution was then neutralizedusing sodium bicarbonate and extracted using dichloromethane; affording substituted indolenineheterocycles 2 which was dried under reduced pressure. The heterocycles 2 were then reacted withan alkyl halide in acetonitrile at 100 C for 12-18 h. The quaternary ammonium salts 3 were precipitatedwith diethyl ether, and collected. |
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