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CAS No. : | 85462-59-5 | MDL No. : | MFCD10698796 |
Formula : | C6H4BrClFN | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | QNKQNJJCNWUOHC-UHFFFAOYSA-N |
M.W : | 224.46 | Pubchem ID : | 11424638 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-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 |
---|---|---|
77% | b) 6-(2-Bromo-5-chloro-4-fluoro-phenV?-4,6-diaza-spiro(at)2.41hentane-5,7-dione; To a solution of 2-bromo-5-chloro-4-fluoroaniline (0.6 g, 2.7 mmol) and triethylamine (0.93 ml, 6.7 mmol) in 20 ml chloroform is added triphosgene (0.32 g, 1.07 mmol) in one portion. After stirring at room temperature for 5 hours first triethylamine (0.45 ml, 3.2 mmol) then 1- aminocyclopropane-1-carboxylic acid ethyl ester x HCI (0,44g, 2.7 mmol) and the mixture is stirred at 65 C for 16 hours. The crude product obtained after aquous workup is dissolved in 20 ml dioxane, potassium carbonate (0.37 g, 2.7 mmol) is added and the mixture heated to 120 C for 16 hours. Addition of water, extraction with ethylacetate, drying and concentration gave the crude hydantoin which is further purified by RP-HPLC to yield 0.69 g (2.1 mmol, 77%) of the title compound. 1 H-NMR (400MHz; DMSO-d6), 8 (ppm) : 1.37 (s, 4H), 7.97 (d, 1 H), 8.04 (d, 1H), 8.71 (s, 1 H). MS (m/z) ESI+: 333 (100, MH+). |
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