ChemicalBook--->CAS DataBase List--->70315-70-7

70315-70-7

70315-70-7 Structure

70315-70-7 Structure
IdentificationBack Directory
[Name]

3-Iodo-6-nitroindazole
[CAS]

70315-70-7
[Synonyms]

Axitinib Intermediate
3-LODO-6-NITROINDAZOLE
3-IODO-6-NITROINDAZOLE
Axitinib Intermediate 1
3-iodo-6-nitro-2h-indazole
3-IODO-6-NITRO (1H)INDAZOLE
1H-Indazole, 3-iodo-6-nitro-
3-Iodo-6-nitro-1H-indazole ,97%
[Molecular Formula]

C7H4IN3O2
[MDL Number]

MFCD07781652
[MOL File]

70315-70-7.mol
[Molecular Weight]

289.03
Chemical PropertiesBack Directory
[Melting point ]

259-261 °C
[Boiling point ]

458.0±25.0 °C(Predicted)
[density ]

2.24
[storage temp. ]

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

powder to crystal
[pka]

9.12±0.40(Predicted)
[color ]

Light yellow to Yellow to Orange
[InChI]

InChI=1S/C7H4IN3O2/c8-7-5-2-1-4(11(12)13)3-6(5)9-10-7/h1-3H,(H,9,10)
[InChIKey]

GZCGNGLOCQEDMT-UHFFFAOYSA-N
[SMILES]

N1C2=C(C=CC([N+]([O-])=O)=C2)C(I)=N1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

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

P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330-P302+P352+P312-P304+P340+P312
[Hazard Codes ]

Xn
[Risk Statements ]

22-60
[Safety Statements ]

53-22-36/37/39-45
[WGK Germany ]

3
[HS Code ]

29339900
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Acetic acid-->N,N-Dimethylformamide-->Sodium nitrite-->Iodine-->2-Methyl-5-nitroaniline-->6-Nitroindazole-->iodine-->Potassium carbonate
[Preparation Products]

(E)-6-Nitro-3-[2-(pyridin-2-yl)ethenyl]-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-->(E)-3-[2-(Pyridin-2-yl)ethenyl]-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-amine
Hazard InformationBack Directory
[Chemical Properties]

Yellow solid
[Uses]

3-Iodo-6-nitroindazole is used as an intermediate in the synthesis of axitinib [6].
[Synthesis]

6-Nitroindazole

7597-18-4

3-Iodo-6-nitroindazole

70315-70-7

General procedure for the synthesis of 3-iodo-6-nitroindazole from 6-nitro-1H-indazole: 6-nitroindazole (45.08 kg) was dissolved in N,N-dimethylformamide (DMF, 228 kg), and powdered potassium carbonate (77 kg) was added while controlling the temperature of the reaction system ≤30°C. The reaction was carried out by slow dropwise addition of iodine (123 kg) solution in DMF (100 kg) over 5 to 6 hours. A solution of iodine (123 kg) dissolved in DMF (100 kg) was added slowly and dropwise over a period of 5 to 6 hours, during which the reaction temperature was maintained at ≤35°C (note: the reaction is exothermic). The reaction mixture was stirred continuously at 22°C for 1 to 5 hours until high performance liquid chromatography (HPLC) monitoring showed that the reaction was complete. Subsequently, the reaction mixture was slowly added to an aqueous solution (455 kg) containing sodium thiosulfate (68 kg) and potassium carbonate (0.46 kg) and the temperature was controlled to be ≤30°C during addition. The mixture was continued to be stirred at 22°C for 1.5 hours. Water (683 kg) was added to precipitate the product and the slurry was stirred at 22°C for 1 to 2 hours. The solid product was collected by filtration, washed with water (2 x 46 kg) and subsequently dried in a vacuum oven at 50 °C and 25 mmHg for 24 to 48 hours to give a yellowish-white solid 3-iodo-6-nitroindazole (74.7 kg, HPLC purity 86.6%, moisture content 0.2%).

[References]

[1] Organic Process Research and Development, 2015, vol. 19, # 7, p. 849 - 857
[2] Patent: WO2009/36066, 2009, A1. Location in patent: Page/Page column 51
[3] Patent: WO2006/48745, 2006, A1. Location in patent: Page/Page column 21
[4] Patent: WO2006/48761, 2006, A2. Location in patent: Page/Page column 30
[5] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 5, p. 1327 - 1333
Spectrum DetailBack Directory
[Spectrum Detail]

3-Iodo-6-nitroindazole(70315-70-7)1HNMR
70315-70-7 suppliers list
Company Name: Jinan XinKe Pharmaceutical Technology Co., Ltd.  Gold
Telephone: 0531-88259693 18660188356
Website: www.zisonpharm.cn/
Company Name: Shanghai YuanQi Biotechnology Co., Ltd.  Gold
Telephone: +86-2332782371 +86-18120098618
Website: www.chemicalbook.com/ShowSupplierProductsList16784/0_EN.htm
Company Name: Sci-Sun Technology CO.,Ltd  Gold
Telephone: 18252089365
Website:
Company Name: Jay Chemicals  Gold
Telephone: 13732234254
Website:
Company Name: Shanghai Haozhu Pharmaceutical Technology Co. , Ltd.  Gold
Telephone: 18912729622
Website: https://www.chemicalbook.com/supplier/25348346/
Company Name: J & K SCIENTIFIC LTD.  
Telephone: 18210857532 18210857532
Website: https://www.jkchemical.com
Company Name: Yangzhou Siyu Chemical Co.,Ltd.  
Telephone: 0514-87325867
Website: www.siyuchem.com
Company Name: PharmaBlock Sciences (Nanjing),Inc.  
Telephone: 025-86918202 4000255188
Website: http://www.pharmablock.com/
Company Name: BeiJing Hwrk Chemicals Limted  
Telephone: 0757-86329057 18934348241
Website: www.hwrkchemical.com/
Company Name: Beijing Ouhe Technology Co., Ltd  
Telephone: 13552068683 13522913783
Website: www.ouhetech.cn/
Company Name: Shanghai Scientia Pharmaceutical Technology Co., Ltd.  
Telephone: 21-21-54301573 13917723525
Website: http://www.scientiapharm.com.cn
Company Name: Adamas Reagent, Ltd.  
Telephone: 4006009262 13023226327
Website: www.tansoole.com
Company Name: Accela ChemBio Co.,Ltd.  
Telephone: 021-50795510 4000665055
Website: http://www.shao-yuan.com/
Company Name: ZEROSCHEM.CO.,LTD.  
Telephone: 10-61256048 13810278579;
Website: http://www.zeroschem.com
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Telephone: 021-50135380
Website: www.shchemsky.com
Company Name: China DongFan Chemical Co.,LTD  
Telephone: 86-0571-85151182
Website: www.chemicalbook.com/ShowSupplierProductsList14819/0_EN.htm
Company Name: Shandong Xiya Chemical Co., Ltd  
Telephone: 13355009207 13355009207
Website: http://www.xiyashiji.com
Company Name: SpringPharma Tech Co.,Ltd  
Telephone: +86-25-68710855, +86-25-68710897
Website: www.springpharma.net
Tags:70315-70-7 Related Product Information
7597-18-4 127-68-4 10102-44-0 606-20-2 75-52-5 100-02-7 98-95-3