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CAS No. : | 767-15-7 | MDL No. : | MFCD00006102 |
Formula : | C6H9N3 | Boiling Point : | - |
Linear Structure Formula : | (C4HN2)(NH2)(CH3)2 | InChI Key : | IDQNBVFPZMCDDN-UHFFFAOYSA-N |
M.W : | 123.16 | Pubchem ID : | 13021 |
Synonyms : |
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Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P280-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302 | Packing Group: | N/A |
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 |
---|---|---|
83% | With N-Bromosuccinimide In acetonitrile at 20℃; for 3 h; Inert atmosphere | 2-Amino-5-bromo-4,6-dimethylpyrimidine (3):; To a stirred solution containing 4.3 lg (34.75 mmol) of 2-amino-4,6-dimethylpyrimidine (2) in 150 mL of acetonitrile were added 6.15g (52.12 mmol) of N-bromosuccinimide. The reaction mixture was stirred at room temperature under argon atmosphere for 3 h. The formed precipitate was filtered and dried to afford the expected product as a white solid: yield 5.93g (83percent).1H-NMR(CDC13) δ 5.19 (br, 2H), 2.44 (s, 6H);13C-NMR (CDC13) δ 166.28, 160.73, 109.60, 24.70. |
83% | With N-Bromosuccinimide In acetonitrile at 23℃; for 3 h; Inert atmosphere | To a stirred solution containing 4.31 g (34.8 mmol) of 2-amino-4,6-dimethylpyrimidine (4) in 150 mL of acetonitrile was added 6.15 g (52.1 mmol) of N-bromosuccinimide. The reaction mixture was stirred at 23 °C for 3 h. The formed precipitate was filtered and dried to afford 5 as a colorless solid: yield 5.93 g (83percent); mp 183-185 °C; silica gel TLC Rf 0.15 (2:1 ethyl acetate/hexanes); 1H NMR (CDCl3) δ 2.44 (s, 6H) and 5.19 (br s, 2H); 13C NMR (CDCl3) δ 24.7, 109.6, 160.7 and 166.3; mass spectrum (APCI), m/z 201.9982 (M+H)+ (C6H9N3Br requires 201.9980). |
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