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| | 2-Amino-3-bromo-5-fluoropyridine Basic information |
| | 2-Amino-3-bromo-5-fluoropyridine Chemical Properties |
| Melting point | 61-63°C | | Boiling point | 63-65℃ | | density | 1.813±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | form | powder to crystal | | pka | 1.86±0.49(Predicted) | | color | White to Almost white | | CAS DataBase Reference | 869557-43-7(CAS DataBase Reference) |
| | 2-Amino-3-bromo-5-fluoropyridine Usage And Synthesis |
| Uses | 2-Amino-3-bromo-5-fluoropyridine is a reactant used in the synthesis of cyano heteroaryl bromides. | | Synthesis | The general procedure for the synthesis of 2-amino-3-bromo-5-fluoropyridine from 2-amino-5-fluoropyridine is as follows:
Method C: Bromination reaction using sulfuric acid (H2SO4). This was done as follows: a solution of 93% sulfuric acid (12.5 kg, 119 mol) in water (26 L) was added to a 50 L reactor, followed by 2-amino-5-fluoropyridine (6.5 kg, 58 mol). The reaction temperature was adjusted to 30 °C and then bromine (10 kg, 63 mol) was added in 10 portions over 3 hours. The reaction mixture was stirred at 45 °C for 18 hours, followed by continued stirring at 50 °C for 5 hours. Upon completion of the reaction, the mixture was cooled to 15 °C and transferred to a 400 L reactor for post-processing.
The products of the four reactions (4 x 6.5 kg) were combined and the reaction was quenched with a mixture of 50% sodium hydroxide (110 kg, 1375 mol) and sodium thiosulfate (1.8 kg, 11.4 mol) in water (100 L) at 50 °C, the quenching process lasted for 1-3 hours. The temperature was adjusted to 32 °C, the slurry was filtered and washed with water (80 L) to give a water-wet crude product (62 kg). The same operation was carried out for the second round of three reactions (3 x 6.5 kg of feedstock) to give a water-wet crude product (41 kg).
The crude product (103 kg) was dissolved (partially insoluble) in toluene (280 kg) at 25-30 °C. After addition of brine (20 kg), phase separation could not be achieved due to the presence of solids. The mixture was filtered through a diatomaceous earth pad, washed with toluene and layered. The organic phase was concentrated to 347 L to remove residual water by azeotropy and used in the subsequent preparation of compound 3a. The product concentration was determined by aliquoting to be 181 g/L in a yield of 62.8 kg. An additional 600 g of product was obtained by extraction of the water/brine layer by ethyl acetate (10 L) and separated, which was treated by filtration through a pad of magnesium salts, evaporation, and hexane grinding. The overall yield was 82%. | | References | [1] Patent: WO2015/73481, 2015, A1. Location in patent: Paragraph 0259-0260 [2] Patent: WO2016/183116, 2016, A1. Location in patent: Paragraph 0251; 0252; 0253 [3] Patent: WO2017/97234, 2017, A1. Location in patent: Paragraph 00405 [4] Patent: WO2011/143366, 2011, A1. Location in patent: Page/Page column 75 [5] Patent: WO2011/143365, 2011, A1. Location in patent: Page/Page column 154 |
| | 2-Amino-3-bromo-5-fluoropyridine Preparation Products And Raw materials |
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