101727-15-5Relevant articles and documents
Preparation method for Selexipag intermediate
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Paragraph 0061-0064, (2019/03/15)
The invention provides a method for preparing a Selexipag intermediate 4-((5,6-diphenyl-2-pyrazinyl)(1-methylethyl)amino)-1-butanol. The method includes protecting 4-isopropylamino n-butyl alcohol byusing a hydroxy protecting group reagent, performs addition with 5,6-diphenyl-2-pyrazinyl trifluoromethanesulfonate, and obtains a target compound by removing protecting groups. The preparation methodis high in yield, low in production cost, mild in condition, simple in operation and suitable for industrial production.
Studies on pyrazines. 35 [1]. An improved synthesis of bromopyrazines from hydroxypyrazines
Sato, Nobuhiro,Narita, Nobuhiko
, p. 783 - 786 (2007/10/03)
The synthesis of bromopyrazines from hydroxypyrazines was successfully effected by the procedure via trimethylsilyloxypyrazines, the sequence of which proceeds under mild conditions and does not require the isolation of intermediate.