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CAS No. : | 24415-66-5 | MDL No. : | MFCD00227619 |
Formula : | C6H5ClN4 | Boiling Point : | No data available |
Linear Structure Formula : | (CH3)C5H2N4Cl | InChI Key : | NOIPEBKPGPZXNR-UHFFFAOYSA-N |
M.W : | 168.58 | Pubchem ID : | 520127 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
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* 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 |
---|---|---|
98% | General procedure: A mixture of 0.001 mol of compound (41a-d or 45), 1 equivalentof the respective 4-amino-N-arylbenzenesulfonamides (44a-g) and3 mL of ethanol was stirred and refluxed (78 C) for 2 h. The reactionmixture was poured into ice water, and the precipitateformed was vacuum filtered and washed with water. The precipitatewas purified by recrystallization from methanol/water (2:1) orchromatography TLC Glass Plates (Merck TLC Silica gel 60 RP-18F254s) in chloroform/methanol (9.5:0.5). After purification, therespective hydrochloride was prepared, and the molecules weresolubilized and stirred for 15 min in a 1:1 solution of HCl/H2O andconcentrated under vacuum [17e19]. |
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