Basic information Safety Supplier Related

1-Boc-3-iodoindazole

Basic information Safety Supplier Related

1-Boc-3-iodoindazole Basic information

Product Name:
1-Boc-3-iodoindazole
Synonyms:
  • 1-Boc-3-iodoindazole
  • 1-Boc-3-iodo-1H-indazole
  • 1H-Indazole-1-carboxylic acid, 3-iodo-, 1,1-diMethylethyl ester
  • tert-butyl 3-iodo-1H-indazole-1-carboxylate
  • N-(tert-Butoxycarbonyl)-3-iodoindazole
  • 3-Iodo-indazole-1-carboxylic acid tert-butyl ester
CAS:
290368-00-2
MF:
C12H13IN2O2
MW:
344.15
Mol File:
290368-00-2.mol
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1-Boc-3-iodoindazole Chemical Properties

Melting point:
117℃
Density 
1.65
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
Appearance
White to off-white Solid
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Safety Information

HS Code 
2933998090
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1-Boc-3-iodoindazole Usage And Synthesis

Synthesis

24424-99-5

66607-27-0

290368-00-2

1. 3-Iodo-1H-indazole (0.2 g, 0.82 mmol), di-tert-butyl dicarbonate (0.2 g, 0.92 mmol) and triethylamine (1 mL) were mixed and placed under ultrasonic radiation for 10 minutes. 2. After completion of the reaction, the reaction mixture was neutralized with 1 M HCl solution. 3. The neutralized solution was extracted using dichloromethane (3 x 30 mL). 4. The organic layers were combined and dried over anhydrous sodium sulfate. 5. Vacuum remove the solvent to give the pure product 3-iodo-1H-indazole-1-carboxylic acid tert-butyl ester as light yellow crystals. Yield: 100%; Melting point: 93-95°C; IR (KBr) ν (cm^-1): 1728 (C=O); 1150 (C-O); 424 (C-I). 1H-NMR (CDCl3) δ (ppm): 8.09 (1H, d, J=8.5 Hz, H-7); 7.55 (1H, t, J=7.8 Hz, H-4); 7.46 (1H, d, J=7.9 Hz, H-6); 7.33 (1H, t, J=7.6 Hz, H-5); 1.71 (9H, s, CH3). 13C-NMR (CDCl3) δ (ppm): 148.35; 139.59; 130.17; 129.98; 124.21; 121.96; 114.56; 102.95; 85.48; 28.18. HRMS (ESI) m/z calculated value C12H13IN2O2 [M+H]+: 344.0022, measured value: 344.0016. For the synthesis of tert-butyl 3-iodo-5-nitro-1H-indazole-1-carboxylate (2b): 1. 3-iodo-5-nitro-1H-indazole (0.2 g, 0.69 mmol), di-tert-butyl dicarbonate (0.17 g, 0.78 mmol) and triethylamine (1 mL) were used as raw materials, and the same procedure as above was followed. 2. 0.27 g of pure product as a pale yellow solid was obtained. Yield: 100%; Melting point: 144-145 °C; IR (KBr) ν (cm^-1): 1744 (C=O); 1528 (NO2).

References

[1] Molecules, 2018, vol. 23, # 8,
[2] Patent: WO2015/58140, 2015, A1. Location in patent: Paragraph 00447
[3] Patent: WO2016/58544, 2016, A1. Location in patent: Paragraph 389; 390
[4] Beilstein Journal of Organic Chemistry, 2013, vol. 9, p. 1501 - 1507
[5] Patent: WO2014/47662, 2014, A2. Location in patent: Paragraph 00283

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