Welcome to chemicalbook!
Chinese English Japanese Germany Korea
010-86108875
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List 2-CHLORO-5-IODO-PYRIDIN-3-YLAMINE
426463-09-4

2-CHLORO-5-IODO-PYRIDIN-3-YLAMINE synthesis

5synthesis methods
2-Chloro-5-iodo-3-nitropyridine

426463-05-0

2-CHLORO-5-IODO-PYRIDIN-3-YLAMINE

426463-09-4

General procedure for the synthesis of 3-amino-2-chloro-5-iodopyridine from 2-chloro-5-iodo-3-nitropyridine: 5-iodo-3-nitro-2-chloropyridine (230 mg, 0.809 mmol), ethanol (1 mL), water (6 drops), and concentrated hydrochloric acid (0.020 mL) were stirred at room temperature for 10 minutes. Subsequently, iron powder (500 mg, 8.95 mmol) was added in small portions and the reaction mixture was heated in an oil bath at 100 °C for 20 min. After completion of the reaction, the iron powder was removed by filtration and the filtrate was washed with ethanol. The ethanol layers were combined and concentrated under reduced pressure. The crude product was purified by fast chromatography using 9:1 hexane:ethyl acetate as eluent to afford 5-iodo-3-amino-2-chloropyridine (190 mg, 92% yield) as a colorless solid with a melting point of 129 °C. 1H NMR (CDCl3) δ (ppm): 4.15 (broad single peak, 2H), 7.34 (double peak, J = 2.0 Hz, 1H), and 7.96 (double peaks, J = 2.0 Hz, 1H); 13C NMR (CDCl3) δ (ppm): 91.41, 129.67, 136.31, 140.77, 143.90. Calculated values for elemental analysis (C5H4N2Cl): C, 23.60; H, 1.58; N, 11.01; Measured values: C, 23.66; H 1.52; N, 10.98.

-

Yield:-

Steps:

Multi-step reaction with 3 steps
1: 68 percent / I2; H5IO6
2: 88 percent / POCl3
3: 91 percent / SnCl2

References:

Zhang, Nanjing;Tomizawa, Motohiro;Casida, John E. [Bioorganic and medicinal chemistry letters,2003,vol. 13,# 3,p. 525 - 528]

2-CHLORO-5-IODO-PYRIDIN-3-YLAMINE Related Search: