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
Questions And AnswerBack Directory
[Uses]

8-Bromo-[1,2,4]thiazo[1,5-a]pyridine-2-amine is a pyridine derivative that can be used as a pharmaceutical synthesis intermediate for pharmaceutical synthesis and experimental research.
Safety DataBack Directory
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
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
1124382-72-4 suppliers list
Company Name: Beijing FYF Chemicals Co., Ltd  Gold
Telephone: 010-57903446 15869909019
Website: http://www.fyfchem.com
Company Name: Adamas Reagent, Ltd.  
Telephone: 4006009262 13023226327
Website: www.tansoole.com
Company Name: Nanjing Chemlin Chemical Co., Ltd  
Telephone: 025-83697070 13770331960
Website: www.echemlin.cn
Company Name: Nan Jing Dirise Chemcial Co.,LTD  
Telephone: 025-52161033 15312098939
Website: www.njdrschem.com
Company Name: Xi’an chemsoar Medical Technology Co., ltd  
Telephone: 029-86538357
Website: www.chemicalbook.com/ShowSupplierProductsList15153/0_EN.htm
Company Name: Wuhan ariel chemical Co., LTD.  
Telephone: 18986259541 18986259541
Website: http://www.3stc.com
Company Name: Shanghai Topbiochem Technology Co., Ltd  
Telephone: 021-58170097
Website: www.topbiochem.com
Company Name: Nanjing Norris-Pharm Technology Co., Ltd  
Telephone: 13901585132
Website:
Company Name: Shanghai Jian Chao Chemical Technology Co., Ltd.  
Telephone: 150-2103-5486 18017383231
Website:
Company Name: SuZhou ShiYa Biopharmaceuticals, Inc.  
Telephone: 86(512)5235 8471 17715136450
Website: www.shiyabiopharm.com
Company Name: Wuhan Kaymke Chemical Co., Ltd.,  
Telephone: 027-87342388 18086026008
Website: www.kmkpharm.cn
Company Name: EnliPharma Technology Co., Ltd  
Telephone: 0551-66399836 18955197623
Website: http://www.enlipharma.com
Company Name: Shanghai Chainpharm Bio-medical Technology Co., Ltd.  
Telephone: +86-021-61727342 13611721451
Website: http://www.chainpharm.com/
Company Name: Bide Pharmatech Ltd.  
Telephone: 400-164-7117 18317119277
Website: www.bidepharm.com
Company Name: ShangHai AmK Pharmaceutical Technology Co., Ltd.  
Telephone: 微信 18019252918 18019252918
Website: www.amkchem.com
Company Name: Nanjing Chalf-Pharm Technology Co., Ltd.  
Telephone: 025-57018978 18251899859
Website: http://www.chalf-pharm.com
Company Name: Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.  
Telephone: 025-66028182 17714375163
Website: www.aikonchem.com
Company Name: Xi'an NewProChem Co.,Ltd.  
Telephone: 15332490153
Website: http://show.chemicalbook.com/newprochem
Tags:1124382-72-4 Related Product Information
1126824-74-5 881658-92-0 625394-66-3 1092304-85-2 475994-60-6 331647-05-3 868362-18-9 497261-38-8 187833-72-3 688363-48-6 953039-63-9 1092500-67-8 1194374-75-8 1245644-46-5 347146-15-0 885271-02-3 331646-98-1 67805-68-9