Reference of 10128-72-0, Adding some certain compound to certain chemical reactions, such as: 10128-72-0, name is Methyl 3-hydroxyisonicotinate,molecular formula is C7H7NO3, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 10128-72-0.
Example A; 3, N-Dihydroxy-isonicotinamide To a stirred suspension of methyl 3-hydroxy-isonicotinate (176 g; 1.15 mol) in water/ice (50/50,1700 mL), was added hydroxylamine hydrochloride (127.9 g; 1.84 mol). The temperature fell to-5 C and then aqueous NAOH solution (454 mL, 28% w/v) was added dropwise keeping the temperature below 5 C during the addition. Hereafter the reaction mixture was stirred at ambient temperature for 1.5 h followed by heating to 60 C. At this temperature the pH was adjusted to 5.4 by the addition of aqueous hydrochloric acid (10 M) at which point a heavy precipitate forms. The reaction mixture was then stirred at ambient temperature followed by cooling to 5 C. THE pH was then adjusted to 4.0 by the addition of aqueous hydrochloric acid (10 M), and then was stirred whilst cold for 1,5 h. The crystals were filtered off, rinsed with water (3 x 100 mL), dried on the filter and then dried further at reduced pressure and 40 C overnight to give 3, N-dihydroxy-isonicotinamide (169.3 g, 96%; HPLC purity 98%) as a white solid. NMR data : H-NMR (DMSO-d6,250 MHz) 8 = 7.55 (1H, d, J=6 Hz); 8.11 (1H, d, J=6 Hz); 8.32 (1H, s); 9.56 (1H, s, broad peak); 11.50 (1H, s, broad peak) ppm.
In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles. 10128-72-0, Methyl 3-hydroxyisonicotinate, other downstream synthetic routes, hurry up and to see.
Reference:
Patent; H. LUNDBECK A/S; WO2005/23820; (2005); A1;,
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