Alternatived Products of [ 1646862-09-0 ]
Product Details of [ 1646862-09-0 ]
CAS No. : | 1646862-09-0 |
MDL No. : | |
Formula : |
C18H16F2N2O6
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Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | - |
M.W : |
394.33
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Pubchem ID : | - |
Synonyms : |
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Safety of [ 1646862-09-0 ]
Signal Word: | |
Class: | |
Precautionary Statements: | |
UN#: | |
Hazard Statements: | |
Packing Group: | |
Application In Synthesis of [ 1646862-09-0 ]
* 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.
- Downstream synthetic route of [ 1646862-09-0 ]
- 1
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[ 1646862-09-0 ]
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[ 1051375-10-0 ]
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[ 1646862-07-8 ]
Yield | Reaction Conditions | Operation in experiment |
|
Multi-step reaction with 3 steps
1: trifluoroacetic acid / acetonitrile / 12 h / 80 °C / Inert atmosphere
2: 1,2-dimethoxyethane / 1 h / 20 °C / Inert atmosphere
3: chloro-trimethyl-silane; sodium iodide / acetonitrile / 5 h / 50 °C / Inert atmosphere |
|
|
Multi-step reaction with 3 steps
1: trifluoroacetic acid / acetonitrile / 16.5 h / 60 °C / Inert atmosphere
2: 1,2-dimethoxyethane / 1 h / 20 °C / Inert atmosphere
3: chloro-trimethyl-silane; sodium iodide / acetonitrile / 5 h / 50 °C / Inert atmosphere |
|
|
Multi-step reaction with 3 steps
1: magnesium triflate / acetonitrile / 21 h / 60 °C / Inert atmosphere
2: 1,2-dimethoxyethane / 1 h / 20 °C / Inert atmosphere
3: chloro-trimethyl-silane; sodium iodide / acetonitrile / 5 h / 50 °C / Inert atmosphere |
|
Reference:
[1]Wang, Huan; Kowalski, Matthew D.; Lakdawala, Ami S.; Vogt, Frederick G.; Wu, Lianming
[Organic Letters, 2015, vol. 17, # 3, p. 564 - 567]
[2]Wang, Huan; Kowalski, Matthew D.; Lakdawala, Ami S.; Vogt, Frederick G.; Wu, Lianming
[Organic Letters, 2015, vol. 17, # 3, p. 564 - 567]
[3]Wang, Huan; Kowalski, Matthew D.; Lakdawala, Ami S.; Vogt, Frederick G.; Wu, Lianming
[Organic Letters, 2015, vol. 17, # 3, p. 564 - 567]
- 2
-
[ 1646862-09-0 ]
-
[ 1051375-10-0 ]
Yield | Reaction Conditions | Operation in experiment |
|
Multi-step reaction with 3 steps
1: trifluoroacetic acid / acetonitrile / 12 h / 80 °C / Inert atmosphere
2: 1,2-dimethoxyethane / 1 h / 20 °C / Inert atmosphere
3: lithium bromide / water; tetrahydrofuran / Reflux |
|
|
Multi-step reaction with 3 steps
1: trifluoroacetic acid / acetonitrile / 16.5 h / 60 °C / Inert atmosphere
2: 1,2-dimethoxyethane / 1 h / 20 °C / Inert atmosphere
3: lithium bromide / water; tetrahydrofuran / Reflux |
|
|
Multi-step reaction with 3 steps
1: magnesium triflate / acetonitrile / 21 h / 60 °C / Inert atmosphere
2: 1,2-dimethoxyethane / 1 h / 20 °C / Inert atmosphere
3: lithium bromide / water; tetrahydrofuran / Reflux |
|
Reference:
[1]Wang, Huan; Kowalski, Matthew D.; Lakdawala, Ami S.; Vogt, Frederick G.; Wu, Lianming
[Organic Letters, 2015, vol. 17, # 3, p. 564 - 567]
[2]Wang, Huan; Kowalski, Matthew D.; Lakdawala, Ami S.; Vogt, Frederick G.; Wu, Lianming
[Organic Letters, 2015, vol. 17, # 3, p. 564 - 567]
[3]Wang, Huan; Kowalski, Matthew D.; Lakdawala, Ami S.; Vogt, Frederick G.; Wu, Lianming
[Organic Letters, 2015, vol. 17, # 3, p. 564 - 567]