6-chloro-5-iodonicotinic acid
6-chloro-5-iodonicotinic acid Basic information
- Product Name:
- 6-chloro-5-iodonicotinic acid
- Synonyms:
-
- 6-chloro-5-iodonicotinic acid
- 6-chloro-5-iodopyridine-3-carboxylic acid
- 6-Chloro-5-iodo-3-pyridinecarboxylic acid
- 5-Iod-6-chlornicotinsaeure
- 6-chloro-5-iodopyridine-3-carboxylicaci
- 3-Pyridinecarboxylic acid, 6-chloro-5-iodo-
- 6-Chloro-5-iodo-pyridin-3-carboxylic acid
- CAS:
- 59782-87-5
- MF:
- C6H3ClINO2
- MW:
- 283.45
- Product Categories:
-
- Carboxylic Acids
- Pyridines
- Mol File:
- 59782-87-5.mol
6-chloro-5-iodonicotinic acid Chemical Properties
- Melting point:
- 196-198°
- Boiling point:
- 411.8±45.0 °C(Predicted)
- Density
- 2.193±0.06 g/cm3 (20 ºC 760 Torr)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 2.89±0.10(Predicted)
- Appearance
- Off-white to light yellow Solid
6-chloro-5-iodonicotinic acid Usage And Synthesis
Synthesis
59782-91-1
59782-87-5
General procedure for the synthesis of 5-iodo-6-chloronicotinic acid from 2-chloro-3-iodo-5-methylpyridine: 2-chloro-3-iodo-5-methylpyridine (4.00 g, 15.8 mmol) was dissolved in water (160 mL), and heated at 80 °C until completely dissolved. Potassium permanganate (6.24 g, 39.5 mmol) was added in batches and the reaction mixture was heated to reflux at 100 °C for 3 hours. Upon completion of the reaction, the hot reaction solution was filtered through Celite 545 and the filter cake was washed with hot water (3 x 20 mL). The filtrates were combined, concentrated to half the original volume and subsequently cooled to 0 °C. The pH was adjusted to 1-2 by slow dropwise addition of concentrated aqueous hydrochloric acid (37%, w/w). the precipitate precipitated was collected by filtration, washed with cold water (2 × 5 mL) and dried in a vacuum desiccator to afford 6-chloro-5-iodonicotinic acid (795 mg, 2.8 mmol) as a white solid in 18% yield. The product characterization data were as follows: thin-layer chromatography Rf value (ethyl acetate/cyclohexane, 5/5, v/v) 0.40; melting point 208-210 °C (literature value: 198-200 °C); infrared spectroscopy (KBr) ν 851, 1283, 1365, 1701, 2400-3100 cm-1; 1H NMR (200 MHz, DMSO-d6) δ 8.65 (d, 1H, J = 2.0 Hz, H-4), 8.83 (d, 1H, J = 2.0 Hz, H-2); 13C NMR (50 MHz, DMSO-d6) δ 96.0 (C-5), 126.9 (C-3), 149.4 (C-4 or C-2), 149.6 (C-4 or C-2), 157.1 (C-6) 164.3 (C=O); ESI-MS m/z 281.87 [M-H]-.
References
[1] European Journal of Medicinal Chemistry, 2015, vol. 92, p. 818 - 838
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6-chloro-5-iodonicotinic acid(59782-87-5)Related Product Information
- 6-chloro-5-(trifluoroMethyl)pyridin-3-yl)Methanol
- 6-Chloro-5-Methylpyridine-2-carboxylic acid
- Methyl 6-chloro-5-(trifluoroMethyl)nicotinate
- 6-CHLORO-5-(TRIFLUOROMETHYL)PYRIDIN-3-AMINE
- 6-CHLORO-5-FLUOROBENZIMIDAZOLE
- Methyl-6-chloro-5-nitronicotinate
- 2-Pyridinamine, 6-chloro-5-methyl
- 2-Pyridinecarboxylic acid, 6-chloro-5-hydroxy-
- Ethyl 2-chloronicotinate
- Ethyl 2,6-dichloro-5-fluoro-pyridine-3-acetoacetate
- 2,5-Dichloronicotnic acid
- METHYL 6-CHLORO-5-IODONICOTINATE
- 5-IODONICOTINIC ACID
- 2-Chloro-3-iodopyridine
- 6-chloro-5-iodonicotinic acid
- (5-IODO-PYRIDIN-3-YL)-METHANOL
- 5-IODO-PYRIDINE-3-CARBALDEHYDE
- 2-CHLORO-3-IODO-5-PICOLINE