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CAS No. : | 57381-56-3 | MDL No. : | MFCD03094168 |
Formula : | C7H3ClFN | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | HBTXAKDVIXNVHZ-UHFFFAOYSA-N |
M.W : | 155.56 | Pubchem ID : | 93656 |
Synonyms : |
|
Signal Word: | Danger | Class: | 6.1 |
Precautionary Statements: | P261-P280-P305+P351+P338-P310 | UN#: | 3439 |
Hazard Statements: | H302-H311-H315-H319-H332 | 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 |
---|---|---|
66% | Preparation 13: 1-[2-ChIoro-5-(4-methyI-piperazin-1-yl)-phenyl]-ethanone; STEP A; A mixture of <strong>[57381-56-3]2-chloro-5-fluoro-benzonitrile</strong> (1 g, 6.43 mmol), K2CO3 (2.66 g, 19.3 mmol) and 1-methyl-piperazine (1.02 g, 10.26 mmol) in DMSO (14 ml) was stirred at 1000C overnight and then further 1-methyl-piperazine (1.02 g, 10.26 mmol) was added. The mixture was stirred at 1000C overnight and then partitioned between water and Et2O. The organic phase was extracted with 1 M HCI and the aqueous layer was brought to basic conditions with NH4OH and extracted with DCM. The organic phase was dried over Na2SO4 and evaporated in vacuo to give 1 g of 2- chloro-5-(4-methyl-piperazin-1-yl)-benzonitrile. Y= 66% |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
77% | With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In 1,4-dioxane; at 75 - 100℃; for 8.08333h;Inert atmosphere; | General procedure: A solution of 2 M Na2CO3 (10 mL) was added under nitrogen to a 2-bromoaniline (10 mmol) in 60 mL dioxane. After 5 min stirring at 75 C, Pd[P(C6H5)3]4 was added followed by (10 mmol) of a 2-cyanophenylboronic acid pinacol ester. The reaction was stirred 8 h at 100 C. After cooling to rt the mixture was vacuum concentrated to half of its initial volume and extracted with CH2Cl2 (30 mL) and water (30 mL). The aqueous phase was extracted with CH2Cl2 (3×20 mL). The combined organic layers were washed with brine, dried over Na2SO4 and evaporated. The solid crystallized upon concentration. |
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