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CAS No. : | 28797-48-0 | MDL No. : | MFCD21648226 |
Formula : | C14H10ClN3O2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | RMBZFWLMYVPNGI-UHFFFAOYSA-N |
M.W : | 287.70 | Pubchem ID : | 120053 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P280-P305+P351+P338-P310 | UN#: | |
Hazard Statements: | H302-H315-H319-H332-H335 | Packing Group: | |
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 |
---|---|---|
58% | With sodium carbonate; In ethanol; | EXAMPLE 10 11-[(1-Ethyl-3-piperidyl)aminoacetyl]-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one 7.2 gm of 11-chloroacetyl-5,11-dihydro-6H-pyrido [2,3-b][1,4]benzodiazepin-6-one, 2.8 gm of sodium carbonate and 3.8 gm of <strong>[6789-94-2]1-ethyl-3-amino-piperidine</strong> were refluxed in 100 ml of ethanol for 5 hours. Then the hot mixture was suction-filtered, the filtrate was evaporated in vacuo to dryness, and the residue was purified on a silica gel column. The evaporation residue of the elude was recrystallized from ethyl acetate. M.p.: 147-148 C. Yield: 58% of theory. |
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