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CAS No. : | 67622-86-0 | MDL No. : | MFCD11043099 |
Formula : | C5H13NO | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | KYCZVVFGMGLNPL-UHFFFAOYSA-N |
M.W : | 103.16 | Pubchem ID : | 13432442 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-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 |
---|---|---|
In methanol; at 100℃; for 0.25h;Microwave irradiation; | EXAMPLE 121 4-[2-tert-Butyl-1-(tetrahydropyran-4-ylmethyl)-1H-imidazol-4-yl]-N-(2-hydroxy-2-methylpropyl)-N-methylthiophene-2-carboxamide (Compound 121) Step 1; 1-Chloro-2-methyl-2-propanol (103 muL, 1.00 mmol) was dissolved in a 40percent methylamine methanol solution (0.5 mL), and the mixture was stirred at 100°C for 15 minutes at 100 W in a microwave-assisted chemical synthesis instrument (CEM Discover). After the mixture was left to cool to room temperature, the solvent was evaporated under reduced pressure. Then, acetonitrile (3 mL) was added to the residue, and the precipitated solid was removed by filtration. After an aqueous sodium hydrogen carbonate solution (10 drops) was added to the filtrate, the solvent was evaporated under reduced pressure to give a roughly purified product of 2-methyl-1-(methylamino)propan-2-ol. The roughly purified product was used in the subsequent step as such without purification. |
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