Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List 2-Amino-5-bromopyrazine

2-Amino-5-bromopyrazine synthesis

7synthesis methods
5049-61-6 Synthesis
Aminopyrazine

5049-61-6
419 suppliers
$8.00/10g

24241-18-7 Synthesis
2-Amino-3,5-dibromopyrazine

24241-18-7
418 suppliers
$6.00/5g

-

Yield:59489-71-3 88% ,24241-18-7 6%

Reaction Conditions:

with N-Bromosuccinimide in acetonitrile at 100; for 0.0833333 h;Microwave irradiation;Solvent;Temperature;

Steps:

Reaction under Microwave Irradiation; General Procedure
General procedure: To a solution of the pyrazine-2-amine (1.0 mmol) in acetonitrile (5 mL) in a glass tube (10 mL) sealed with a silicon septum was added N-iodosuccinimide (NIS) (procedure A) (1.1–3.0 mmol)or I2 (1.1 mmol) or N-chlorosuccinimide (NCS) (procedure B) orN-bromosuccinimide (NBS) (procedure C) (1.1–2.2 mmol) containing magnetic stirring. The tube was introduced to the microwave oven, heated to 100 °C, and subjected to a variable MW power until 300 W (an IR sensor measured the temperature of the glass tube surface) until no starting material couldbe detected by thin-layer chromatography. Then, the solvent was removed under reduced pressure to give the crude product,which was purified by silica gel column chromatography. Alternatively, the crude reaction mixture can be extracted with diethyl ether/water (3×15 mL), dried with sodium sulfate, filtered,and the solvent can be removed to dryness. Representative product:

References:

Grima, Josep;Lizano, Enric;Pujol, M. Dolors [Synlett,2019,vol. 30,# 17,p. 2000 - 2003]

FullText

2-Amino-5-bromopyrazine Related Search: