1-Boc-3-iodoindazole
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
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
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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