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ChemicalBook--->CAS DataBase List--->886860-50-0

886860-50-0

886860-50-0 Structure

886860-50-0 Structure
IdentificationBack Directory
[Name]

2-AMINO-5-IODOPYRAZINE
[CAS]

886860-50-0
[Synonyms]

5-iodopyrazin-2-aMine
5-iodo-2-Pyrazinamine
2-AMINO-5-IODOPYRAZINE
2-Pyrazinamine, 5-iodo-
[Molecular Formula]

C4H4IN3
[MDL Number]

MFCD09909691
[MOL File]

886860-50-0.mol
[Molecular Weight]

221
Chemical PropertiesBack Directory
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[Appearance]

Light yellow to brown Solid
[InChI]

InChI=1S/C4H4IN3/c5-3-1-8-4(6)2-7-3/h1-2H,(H2,6,8)
[InChIKey]

VVTVALQVXWRFAM-UHFFFAOYSA-N
[SMILES]

C1(N)=NC=C(I)N=C1
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2-AMINO-5-IODOPYRAZINE(886860-50-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Aminopyrazine

5049-61-6

2-AMINO-5-IODOPYRAZINE

886860-50-0

To a 1000 mL single neck round bottom flask was added 2-aminopyrazine (28.50 g, 300 mmol) and N-iodosuccinimide (134.99 g, 600 mmol) followed by methanol (340 mL). The reaction mixture was stirred at 80 °C for 10 hours. The reaction progress was monitored by thin layer chromatography (TLC) and gas chromatography (GC) to confirm the completion of the reaction. Upon completion of the reaction, the solvent was removed using a rotary evaporator to obtain the crude product. The crude product was purified by silica gel column chromatography to obtain the target compound 2-amino-5-iodopyrazine. The product was dried and the yield was calculated to be 70.50% and analyzed by high performance liquid chromatography (HPLC) with a purity of 99.58%.

[References]

[1] Patent: CN106674137, 2017, A. Location in patent: Paragraph 0009-0011; 0012-0014; 0015-0016
[2] Heterocycles, 2012, vol. 86, # 2, p. 1323 - 1339
[3] Patent: JP2015/54838, 2015, A. Location in patent: Paragraph 0083; 0084
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