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CAS No. : | 6780-38-7 | MDL No. : | MFCD00192872 |
Formula : | C10H6ClNO3 | Boiling Point : | - |
Linear Structure Formula : | C6H4(C2O2NCH2C(O)Cl) | InChI Key : | RHZBRCQIKQUQHQ-UHFFFAOYSA-N |
M.W : | 223.61 | Pubchem ID : | 81242 |
Synonyms : |
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Signal Word: | Danger | Class: | 8,6.1 |
Precautionary Statements: | P280-P301+P310-P305+P351+P338-P310 | UN#: | 2923 |
Hazard Statements: | H301-H314 | Packing Group: | Ⅲ |
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 |
---|---|---|
General procedure: To a suspension of N-phthaloylglycine 5 (1.0 equiv) in chloroform (0.2 M) was added thionyl chloride (1.5 equiv). The reaction mixture was refluxed for 4 hours, after which the solution was concentrated in vacuo. The mixture was then taken in THF (0.4 M) and cooled down to 0C in an ice bath. To this was added a solution of the suitably functionalized aniline 6a-e (1.2 equiv) and triethylamine (2.0M) in THF (0.4 M). The reaction mixture was then refluxed overnight, following which it was diluted with ethyl acetate and washed subsequently with 1N HCl and saturated NaHCO3. The ethyl acetate layer was concentrated in vacuo and the crude was used in the next step without purification. |