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5-Bromo-4-hydrazinyl-2,6-dimethylpyrimidine synthesis

3synthesis methods
69696-35-1 Synthesis
5-Bromo-4-chloro-2,6-dimethylpyrimidine

69696-35-1
38 suppliers
$69.00/100mg

5-Bromo-4-hydrazinyl-2,6-dimethylpyrimidine

69696-36-2
9 suppliers
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Yield:69696-36-2 91%

Reaction Conditions:

with hydrazine hydrate in methanol;ethanol at 0 - 20; for 16 h;

Steps:

B1.3 5-Bromo-4-hydrazinyl-2,6-dimethylpyrimidine (B1.3)

5-Bromo-4-hydrazinyl-2,6-dimethylpyrimidine (B1.3) (0349) To a mixture of Hydrazine hydrate (NH2NH2.H2O, 32 g, 0.64 mol, 98%) in 350 mL ethanol was added a solution of B1.2 (70 g, 0.32 mol) in 350 mL methanol dropwise at 0° C. The reaction mixture was stirred at rt for 16 h. The solvent was removed by reduced pressure, the residue was diluted with 500 mL of water, extracted with CHCl3 (500 mL×3). The combined organic layers were washed with 500 mL brine, dried over Na2SO4, and concentrated to give the title compound (63 g, 91%) as a yellow solid. LC-MS: [M+H]+=219.0.

References:

US2016/176882,2016,A1 Location in patent:Paragraph 0346; 0349