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ChemicalBook--->CAS DataBase List--->1124382-72-4

1124382-72-4

1124382-72-4 Structure

1124382-72-4 Structure
IdentificationBack Directory
[Name]

8-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine
[CAS]

1124382-72-4
[Synonyms]

106347
EOS-61162
8-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine
2-AMino-8-broMo[1,2,4]triazolo[1,5-a]pyridine
8-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine
[1,2,4]Triazolo[1,5-a]pyridin-2-amine, 8-bromo-
8-bromo - [1,2,4] thiazolo [1,5-a] pyridine-2-amine
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C6H5BrN4
[MDL Number]

MFCD16658939
[MOL File]

1124382-72-4.mol
[Molecular Weight]

213.035
Chemical PropertiesBack Directory
[density ]

2.09
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

solid
[pka]

3.83±0.30(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C6H5BrN4/c7-4-2-1-3-11-5(4)9-6(8)10-11/h1-3H,(H2,8,10)
[InChIKey]

SUFKKFLJJMKVJJ-UHFFFAOYSA-N
[SMILES]

C12=NC(N)=NN1C=CC=C2Br
Safety DataBack Directory
[WGK Germany ]

3
Spectrum DetailBack Directory
[Spectrum Detail]

8-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine(1124382-72-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

ethyl {[(3-broMopyridin-2-yl)aMino]carbonothioyl}carbaMate

1124383-00-1

8-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine

1124382-72-4

The general procedure for the synthesis of 2-amino-8-bromo[1,2,4]triazolo[1,5-a]pyridine from compound (CAS:1124383-00-1) is as follows: 1. Dissolution step: Methanol (MeOH, 300 mL), hydroxylamine hydrochloride (62.83 g, 904 mmol) and diisopropylethylamine (DIPEA, 694 mL, 543 mmol) were added to a solution of Intermediate 50 (55 g, 181 mmol) in ethanol (EtOH, 300 mL). 2. Reaction step: the reaction mixture was stirred at room temperature (r.t.) for 6 hours. 3. Post-treatment step: the reaction mixture was concentrated in vacuum and the residue was suspended in diisopropyl ether (DIPE). 4. Separation step: the precipitate was collected by filtration. 5. 5. Yield: 51 37 g of intermediate were obtained in 96% yield.

[References]

[1] Patent: WO2013/10904, 2013, A1. Location in patent: Page/Page column 76
[2] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 17, p. 4794 - 4800
[3] Patent: KR2015/77599, 2015, A. Location in patent: Paragraph 0096; 0099-0101
[4] Patent: KR101601354, 2016, B1. Location in patent: Paragraph 0110 - 0112
[5] Patent: US2011/190269, 2011, A1. Location in patent: Page/Page column 66
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