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CAS No. : | 74654-07-2 | MDL No. : | MFCD17215909 |
Formula : | C7H17NO3 | Boiling Point : | No data available |
Linear Structure Formula : | H2NCH2CH2OCH2CH2OCH2CH2OCH3 | InChI Key : | OKUWOEKJQRUMBW-UHFFFAOYSA-N |
M.W : | 163.21 | Pubchem ID : | 3018531 |
Synonyms : |
|
Chemical Name : | 2-(2-(2-Methoxyethoxy)ethoxy)ethanamine |
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 |
---|---|---|
at 120℃; for 1h;Microwave irradiation; | General procedure: 4-(Chloromethyl)-N-(4-(methyl-3-(4-(pyridin-3-yl)pyrimidine-2-ylamino)phenyl)benzamide (129 mg, 0.3 mmol) and mPEGn-NH2 (1.50 mmol, n=3, 5, 7, 9) was reacted under microwave conditions at 120C for one hour. After cooling to room temperature, DCM (100 mL) was added to the reaction mixture. The resulting solution was extracted with 1M HCl (50 mL). The acidic aqueous phase was neutralized with sodium carbonate, and then extracted with DCM (100 mL×2). The organic phase was dried over Na2SO4 and the solvent removed under reduced pressure. The resulting residue was purified by column chromatography (biotage: DCM/CH3OH, CH3OH, 5-10%, 25 CV). The desired products were obtained in yields: 65-85%. mPEG3-N-Imatinib (compound la) NMR (500 MHz, CDCl3) delta 2.27 (s, 3H), 2.62 (br., 1H), 2.76 (t, 2H), 3.31 (s, 3H), 3.49 (m, 2H), 3.59 (m, 8H), 3.80 (s, 2H), 7.08 (s, 1H), 7.12 (m, 1H), 7.28 (m, IH), 7.30 (m, 3H), 7.79 (d, 2H), 8.42 (m, 2H), 8.51(d, 2H), 8.62 (d, 1H), 9.17 (s, 1H); LC-MS (m/z) calculated, 556.3, found, 557.3 [M+H]+. |
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