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ChemicalBook CAS DataBase List 2,5-Dibromopyrazine

2,5-Dibromopyrazine synthesis

3synthesis methods
5-bromopyrazin-2-amine (3 g, 17.241 mmol) and bromine (8.2 g, 51.729 mmol) were added to aq. HBr solution at -15° C. Aq. solution of sodium nitrite (2.97 g, 43.0103 mmol) was then added to the mixture over a period of 1 h at -10° C. keeping the internal temperature below 5° C. during addition and stirred for 1 h at 0° C. Progress of reaction was monitored by TLC. After reaction completion reaction mass neutralised with 40percent NaOH solution and extracted with diethyl ether. The organic layer was dried over sodium sulphate and concentrated under reduced pressure (below 30° C.) to yield 2,5-Dibromopyrazine (1 g, 24.4percent) as brown oil.
59489-71-3 Synthesis
2-Amino-5-bromopyrazine

59489-71-3
386 suppliers
$5.00/1g

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Yield:23229-26-7 24.4%

Reaction Conditions:

with hydrogen bromide;bromine;sodium nitrite in water at -15 - 0; for 2 h;

Steps:

32.2 Step 2: Synthesis of 2,5-dibromopyrazine
Step 2:
Synthesis of 2,5-dibromopyrazine
5-bromopyrazin-2-amine (3 g, 17.241 mmol) and bromine (8.2 g, 51.729 mmol) were added to aq. HBr solution at -15° C. Aq. solution of sodium nitrite (2.97 g, 43.0103 mmol) was then added to the mixture over a period of 1 h at -10° C. keeping the internal temperature below 5° C. during addition and stirred for 1 h at 0° C.
Progress of reaction was monitored by TLC.
After reaction completion reaction mass neutralised with 40% NaOH solution and extracted with diethyl ether.
The organic layer was dried over sodium sulphate and concentrated under reduced pressure (below 30° C.) to yield 2,5-dibromopyrazine (1 g, 24.4%) as brown oil.
MS: 238.8[M++1]

References:

Mankind Pharma Ltd.;Patil, Rakesh Ishwar;Verma, Jeevan;Shah, Dharmesh;Ali, Sazid;Bapuram, Srinivasa Reddy;Rai, Santosh Kumar;Kumar, Anil US2017/291910, 2017, A1 Location in patent:Paragraph 0592-0594

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