ChemicalBook--->CAS DataBase List--->153800-11-4

153800-11-4

153800-11-4 Structure

153800-11-4 Structure
IdentificationBack Directory
[Name]

2-ethynylpyrazine
[CAS]

153800-11-4
[Synonyms]

2-ethynylpyrazine
Pyrazine, 2-ethynyl-
2-Ethynylpyrazine 98%
2-Ethynyl-1,4-diazine, (Pyrazin-2-yl)acetylene
[Molecular Formula]

C6H4N2
[MDL Number]

MFCD13189804
[MOL File]

153800-11-4.mol
[Molecular Weight]

104.11
Chemical PropertiesBack Directory
[Boiling point ]

180.3±20.0 °C(Predicted)
[density ]

1.11±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

crystalline solid
[pka]

-0.40±0.10(Predicted)
[color ]

Light gold to faint brown
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P261-P271-P280
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2-ethynylpyrazine(153800-11-4)1HNMR
2-ethynylpyrazine(153800-11-4)FT-IR
Hazard InformationBack Directory
[Synthesis]

2-[2-(trimethylsilyl)ethynyl]pyrazine

291763-66-1

2-ethynylpyrazine

153800-11-4

To a solution of compound (CAS:291763-66-1) (3.0 g, 17.02 mmol) in THF (10 mL) was slowly added 1 M TBAF (tetrabutylammonium fluoride) solution over 9 min. The progress of the reaction was monitored by TLC (Thin Layer Chromatography) to confirm the complete conversion of the feedstock to the target product 2-alkynylpyrazines. After completion of the reaction, the mixture was concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography to give 2-alkynylpyrazines (1.0 g, yield: 56.5%). LC-MS (Liquid Chromatography-Mass Spectrometry) analysis showed: m/z 105 ([M+H]+).

[References]

[1] Patent: WO2017/117708, 2017, A1. Location in patent: Page/Page column 18; 19
[2] Patent: WO2017/93544, 2017, A1. Location in patent: Page/Page column 97; 98
[3] Carbohydrate Research, 2011, vol. 346, # 9, p. 1083 - 1092
[4] Journal of Medicinal Chemistry, 2013, vol. 56, # 7, p. 3033 - 3047
[5] Journal of Medicinal Chemistry, 2016, vol. 59, # 7, p. 3532 - 3548
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