| Identification | Back Directory | [Name]
5-CHLORO-1,3-DIHYDRO-2H-IMIDAZO[4,5-B]PYRIDIN-2-ONE | [CAS]
40851-98-7 | [Synonyms]
5-Chloro-1H-imidazo[4,5-b]pyridin-2(3H) 5-Chloro-1H-iMidazo[4,5-b]pyridin-2(3H)-one 5-chloro-1H,2H,3H-iMidazo[4,5-b]pyridin-2-one 5-Chloro-1,3-dihydro-iMidazo[4,5-b]pyridin-2-one 5-CHLORO-1,3-DIHYDRO-2H-IMIDAZO[4,5-B]PYRIDIN-2-ONE 2H-Imidazo[4,5-b]pyridin-2-one, 5-chloro-1,3-dihydro- | [Molecular Formula]
C6H4ClN3O | [MDL Number]
MFCD06659688 | [MOL File]
40851-98-7.mol | [Molecular Weight]
169.57 |
| Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of 5-chloro-1H-imidazo[4,5-B]pyridin-2(3H)-one from 6-chloro-2,3-diaminopyridine and triphosgene was as follows: 0.143 g (1 mmol) of 6-chloro-pyridine-2,6-diamine was dissolved in 2 ml of methylene chloride, 0.4 g of sodium hydroxide dissolved in 2 ml of water was added to the solution, followed by 0.22 g of triphosgene dissolved in a a solution of 2 ml of dichloromethane. The reaction mixture was treated according to similar literature methods. Colorless crystal product was obtained by ethanol recrystallization. The yield was 0.08 g (0.47 mmol) in 47% yield with a melting point of 374°C. Infrared spectra (IR, cm-1): 3094, 3002, 2817, 1770. 1H NMR (200 MHz, DMSO-d6) δ (ppm): 11.58 (s, 1H, NH), 11.03 (s, 1H, NH), 7.27 (d, 1H, J=8.0 Hz, aromatic H), 7.01 (d, 1H, J= 8.1 Hz, aromatic H).13C NMR (50 MHz, DMSO-d6) δ (ppm): 154.20, 144.34, 139.82, 122.81, 117.08, 115.63. | [References]
[1] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 12, p. 3669 - 3677 |
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