ChemicalBook--->CAS DataBase List--->356560-80-0

356560-80-0

356560-80-0 Structure

356560-80-0 Structure
IdentificationBack Directory
[Name]

6-BROMO-[1,2,4]TRIAZOLO[1,5-A]PYRIDINE
[CAS]

356560-80-0
[Synonyms]

6-BroMo[1,2,4]triazolo[1,...
6-Bromo[1,2,4]triazolo[1,5-α]pyridine
6-BROMO-[1,2,4]TRIAZOLO[1,5-A]PYRIDINE
[1,2,4]Triazolo[1,5-a]pyridine,6-broMo-
6-Bromo[1,2,4]triazolo[1,5-a]pyridine 96%
6-BROMO-[1,2,4]TRIAZOLO[1,5-A]PYRIDINE ISO 9001:2015 REACH
[Molecular Formula]

C6H4BrN3
[MDL Number]

MFCD08689534
[MOL File]

356560-80-0.mol
[Molecular Weight]

198.02
Chemical PropertiesBack Directory
[Melting point ]

100-102
[density ]

1.89±0.1 g/cm3(Predicted)
[storage temp. ]

Keep Cold
[form ]

Solid
[pka]

1.46±0.30(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C6H4BrN3/c7-5-1-2-6-8-4-9-10(6)3-5/h1-4H
[InChIKey]

CXRXKDSDRWLKTK-UHFFFAOYSA-N
[SMILES]

C12=NC=NN1C=C(Br)C=C2
Hazard InformationBack Directory
[Chemical Properties]

Off-white powder
[Uses]

A selective inhibitor of ALK5 kinase
[Synthesis]

(E)-N'-(5-bromopyridin-2-yl)-N,N-dimethylformimidamide

138888-98-9

6-BROMO-[1,2,4]TRIAZOLO[1,5-A]PYRIDINE

356560-80-0

General procedure: N'-(5-bromo-2-pyridinyl)-N,N-dimethylformamidine (4 g, 17.54 mmol, 1.00 eq.) was dissolved in methanol (40 mL) under nitrogen protection and cooled to 0 °C. Subsequently, pyridine (4 mL, 2.00 eq.) and aminoxysulfonic acid (3.6 g, 31.83 mmol, 1.30 eq.) were added sequentially. The reaction mixture was stirred at room temperature for 12 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was diluted with ethyl acetate (150 mL) and washed sequentially with saturated aqueous sodium carbonate solution (50 mL x 1) and water (50 mL x 2). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography with the eluent of ethyl acetate/hexane (1:1) to afford 6-bromo-[1,2,4]triazolo[1,5-A]pyridine 2.5 g (72% yield) as a solid. LC/MS (Method D, ESI): retention time = 1.1 min, m/z = 198.0 [M+H]+.

[References]

[1] Patent: WO2013/127266, 2013, A1. Location in patent: Page/Page column 141
[2] Patent: WO2013/127267, 2013, A1. Location in patent: Page/Page column 92
[3] Patent: WO2013/127268, 2013, A1. Location in patent: Page/Page column 67
[4] Patent: WO2013/130935, 2013, A1. Location in patent: Paragraph 0206
[5] Patent: WO2013/130943, 2013, A1. Location in patent: Paragraph 0214
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22-36/37/38
[Safety Statements ]

26-24/25
[WGK Germany ]

3
[Hazard Note ]

Harmful/Irritant/Keep Cold
[HS Code ]

29349990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Spectrum DetailBack Directory
[Spectrum Detail]

6-BROMO-[1,2,4]TRIAZOLO[1,5-A]PYRIDINE(356560-80-0)1HNMR
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